A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674599



Internal ID15411251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2193611..2210866hg38UCSC Ensembl
Innerchr8:2141142..2158537hg19UCSC Ensembl
Innerchr8:2128549..2145944hg18UCSC Ensembl
Innerchr8:2128549..2145944hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3817256
hg1917396
hg1817396
hg1717396
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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