A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665508



Internal ID15402160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136851516hg38UCSC Ensembl
Innerchr8:137687955..137863759hg19UCSC Ensembl
Innerchr8:137757137..137932941hg18UCSC Ensembl
Innerchr8:137757137..137932941hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38175805
hg19175805
hg18175805
hg17175805
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515708
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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