A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703462



Internal ID15093428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9657865..9670519hg38UCSC Ensembl
Innerchr2:9797994..9810648hg19UCSC Ensembl
Innerchr2:9715445..9728099hg18UCSC Ensembl
Innerchr2:9748592..9761246hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3812655
hg1912655
hg1812655
hg1712655
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527083
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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