A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528929



Internal ID15109536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:170815681..170821869hg38UCSC Ensembl
Innerchr2:171672191..171678379hg19UCSC Ensembl
Innerchr2:171380437..171386625hg18UCSC Ensembl
Innerchr2:171497698..171503886hg17UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg386189
hg196189
hg186189
hg176189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705619
Samples
Known GenesGAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528929
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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