A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697429



Internal ID15434081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121453371..121454187hg38UCSC Ensembl
Innerchr8:122465611..122466427hg19UCSC Ensembl
Innerchr8:122534792..122535608hg18UCSC Ensembl
Innerchr8:122534792..122535608hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38817
hg19817
hg18817
hg17817
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520451
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697429
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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