A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697170



Internal ID15433822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79146817..79163147hg38UCSC Ensembl
Innerchr15:79439159..79455489hg19UCSC Ensembl
Innerchr15:77226214..77242544hg18UCSC Ensembl
Innerchr15:77226214..77242544hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3816331
hg1916331
hg1816331
hg1716331
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519998
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697170
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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