A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698222



Internal ID15434874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35801621..35811457hg38UCSC Ensembl
Innerchr2:36026687..36036523hg19UCSC Ensembl
Innerchr2:35880191..35890027hg18UCSC Ensembl
Innerchr2:35938338..35948174hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg389837
hg199837
hg189837
hg179837
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519867
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698222
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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