A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702192



Internal ID15438844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85495291..85503730hg38UCSC Ensembl
Innerchr8:86407520..86415959hg19UCSC Ensembl
Innerchr8:86594772..86603211hg18UCSC Ensembl
Innerchr8:86594772..86603211hg17UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg388440
hg198440
hg188440
hg178440
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525974
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702192
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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