A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520038



Internal ID15447331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75092517..75097292hg38UCSC Ensembl
Innerchr8:76004752..76009527hg19UCSC Ensembl
Innerchr8:76167307..76172082hg18UCSC Ensembl
Innerchr8:76167307..76172082hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg384776
hg194776
hg184776
hg174776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697190
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520038
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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