A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667302



Internal ID15403954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1959689..1964968hg38UCSC Ensembl
Innerchr8:1907855..1913134hg19UCSC Ensembl
Innerchr8:1895262..1900541hg18UCSC Ensembl
Innerchr8:1895262..1900541hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg385280
hg195280
hg185280
hg175280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517213
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667302
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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