A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522503



Internal ID15449796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:76094160..76147246hg38UCSC Ensembl
Innerchr8:77006395..77059481hg19UCSC Ensembl
Innerchr8:77168950..77222036hg18UCSC Ensembl
Innerchr8:77168950..77222036hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3853087
hg1953087
hg1853087
hg1753087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705871
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522503
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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