Product Details

Assay Reference Genome
Location

Chr.2:51064751 on build GRCh38
Cytoband
2p16.3
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs77634008,rs77820775] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Target Gene Details

Entrez Gene ID
730100
Gene Symbol
LOC730100
Gene Name
uncharacterized LOC730100
Gene Aliases
Location
Chr.2:51032601-52407917 on build GRCh38
Assay Gene Location
Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
LOC730100 NR_135237.1
AK127244.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1000086 Chr2:50879876 - 51193400 on Build GRCh38 Loss NRXN1 LOC730100
esv2759048 Chr2:51054576 - 51138744 on Build GRCh38 Gain LOC730100
nsv2725 Chr2:51046194 - 51067339 on Build GRCh38 Insertion LOC730100
nsv581868 Chr2:51053379 - 51125305 on Build GRCh38 Loss LOC730100
nsv521850 Chr2:51052256 - 51210278 on Build GRCh38 Loss LOC730100
dgv3814n100 Chr2:51044124 - 51123977 on Build GRCh38 Loss LOC730100
nsv1012208 Chr2:51039660 - 51188856 on Build GRCh38 Loss LOC730100
esv3892237 Chr2:51020156 - 51130764 on Build GRCh38 Loss NRXN1 LOC730100
dgv6866n54 Chr2:50820175 - 51108720 on Build GRCh38 Loss NRXN1 LOC730100
nsv581848 Chr2:50711821 - 51118377 on Build GRCh38 Loss NRXN1 LOC730100
nsv581853 Chr2:50786509 - 51326909 on Build GRCh38 Loss NRXN1 LOC730100
esv2763321 Chr2:50610356 - 51126248 on Build GRCh38 Loss NRXN1 LOC730100 MIR8485
esv3892215 Chr2:50887566 - 51133529 on Build GRCh38 Loss NRXN1 LOC730100
nsv834014 Chr2:50954708 - 51133399 on Build GRCh38 Loss NRXN1 LOC730100
nsv1002086 Chr2:50685023 - 51177923 on Build GRCh38 Loss NRXN1 LOC730100 MIR8485

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