A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706011



Internal ID15442663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24183151..24361585hg38UCSC Ensembl
Innerchr15:24428298..24606732hg19UCSC Ensembl
Innerchr15:21979391..22157825hg18UCSC Ensembl
Innerchr15:21979391..22157825hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38178435
hg19178435
hg18178435
hg17178435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706011
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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