A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698237



Internal ID15434889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19898447..19951056hg38UCSC Ensembl
Innerchr2:20098208..20150817hg19UCSC Ensembl
Innerchr2:19961689..20014298hg18UCSC Ensembl
Innerchr2:20019836..20072445hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3852610
hg1952610
hg1852610
hg1752610
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521619
Supporting Variants
Samples
Known GenesTTC32, WDR35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698237
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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