A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695500



Internal ID15432152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:156941324..156981358hg38UCSC Ensembl
Innerchr2:157797836..157837870hg19UCSC Ensembl
Innerchr2:157506082..157546116hg18UCSC Ensembl
Innerchr2:157623344..157663378hg17UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3840035
hg1940035
hg1840035
hg1740035
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518087
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695500
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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