A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700176



Internal ID15436828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70151046..70159197hg38UCSC Ensembl
Innerchr15:70443385..70451536hg19UCSC Ensembl
Innerchr15:68230439..68238590hg18UCSC Ensembl
Innerchr15:68230439..68238590hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388152
hg198152
hg188152
hg178152
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524277
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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