A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524185



Internal ID15451478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:235987877..236013680hg38UCSC Ensembl
Innerchr2:236896521..236922324hg19UCSC Ensembl
Innerchr2:236561260..236587063hg18UCSC Ensembl
Innerchr2:236678521..236704324hg17UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3825804
hg1925804
hg1825804
hg1725804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700067
Samples
Known GenesAGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524185
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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