A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671382



Internal ID15408034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133615160..133631295hg38UCSC Ensembl
Innerchr8:134627403..134643538hg19UCSC Ensembl
Innerchr8:134696585..134712720hg18UCSC Ensembl
Innerchr8:134696585..134712720hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3816136
hg1916136
hg1816136
hg1716136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520436
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671382
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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