A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522737



Internal ID15103344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:184301745..185428608hg38UCSC Ensembl
Innerchr2:185166472..186293335hg19UCSC Ensembl
Innerchr2:184874717..186001580hg18UCSC Ensembl
Innerchr2:184991978..186118841hg17UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381126864
hg191126864
hg181126864
hg171126864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv232n21
Supporting Variantsnssv698371
Samples
Known GenesZNF804A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522737
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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