A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657124



Internal ID15393776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2378491..2725223hg38UCSC Ensembl
Innerchr8:2321764..2582764hg19UCSC Ensembl
Innerchr8:2309171..2570171hg18UCSC Ensembl
Innerchr8:2309171..2570171hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38346733
hg19261001
hg18261001
hg17261001
Variant TypeCNV gain
Copy Number
Allele State
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)nssv657124
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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