A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695269



Internal ID15431921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136785663..136785890hg38UCSC Ensembl
Innerchr8:137797906..137798133hg19UCSC Ensembl
Innerchr8:137867088..137867315hg18UCSC Ensembl
Innerchr8:137867088..137867315hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38228
hg19228
hg18228
hg17228
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)nssv695269
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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