A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695784



Internal ID15432436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161082328..161092788hg38UCSC Ensembl
Innerchr2:161938839..161949299hg19UCSC Ensembl
Innerchr2:161647085..161657545hg18UCSC Ensembl
Innerchr2:161764346..161774806hg17UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3810461
hg1910461
hg1810461
hg1710461
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518357
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695784
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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