A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680219



Internal ID15416871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2489783..2738578hg38UCSC Ensembl
Innerchr8:2346899..2596106hg19UCSC Ensembl
Innerchr8:2334306..2583513hg18UCSC Ensembl
Innerchr8:2334306..2583513hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38248796
hg19249208
hg18249208
hg17249208
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)nssv680219
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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