A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516943



Internal ID15444236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114550093..114591430hg38UCSC Ensembl
Innerchr8:115562322..115603659hg19UCSC Ensembl
Innerchr8:115631498..115672835hg18UCSC Ensembl
Innerchr8:115631498..115672835hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3841338
hg1941338
hg1841338
hg1741338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687276, nssv655104
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516943
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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