Product Details

Assay Reference Genome
Location

Chr.X:31139020 on build GRCh38
Cytoband
Xp21.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
1756
Gene Symbol
DMD
Gene Name
dystrophin
Gene Aliases
BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85
Location
Chr.X:31119219-33339609 on build GRCh38
Assay Gene Location
Within Intron 85
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
DMD NM_000109.3 NP_000100.2
NM_004006.2 NP_003997.1
NM_004009.3 NP_004000.1
NM_004010.3 NP_004001.1
NM_004011.3 NP_004002.2
NM_004012.3 NP_004003.1
NM_004013.2 NP_004004.1
NM_004014.2 NP_004005.1
NM_004015.2 NP_004006.1
NM_004016.2 NP_004007.1
NM_004017.2 NP_004008.1
NM_004018.2 NP_004009.1
NM_004020.3 NP_004011.2
NM_004021.2 NP_004012.1
NM_004022.2 NP_004013.1
NM_004023.2 NP_004014.1
XM_006724468.2 XP_006724531.1
XM_006724469.3 XP_006724532.1
XM_006724470.3 XP_006724533.1
XM_006724473.2 XP_006724536.1
XM_006724474.3 XP_006724537.1
XM_006724475.2 XP_006724538.1
XM_011545467.1 XP_011543769.1
XM_017029328.1 XP_016884817.1
XM_017029331.1 XP_016884820.1
AB208836.1 BAD92073.1
AK299936.1
BC028720.1 AAH28720.1
BC070078.1 AAH70078.1
BC094758.1 AAH94758.1
BC127103.1
BC150141.1
KU178030.1
KU178031.1
KU178032.1
KU178033.1
KU178034.1
M18533.1 AAA53189.1
M92650.1 AAA52316.1
X14298.1 CAA32479.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
esv2661363 ChrX:31137680 - 31139688 on Build GRCh38 Deletion DMD

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