A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523406



Internal ID15450699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102486830..102500824hg38UCSC Ensembl
Innerchr2:103103289..103117283hg19UCSC Ensembl
Innerchr2:102469721..102483715hg18UCSC Ensembl
Innerchr2:102561807..102575801hg17UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3813995
hg1913995
hg1813995
hg1713995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699157
Samples
Known GenesSLC9A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523406
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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