A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522697



Internal ID15449990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:76873211..76880107hg38UCSC Ensembl
Innerchr8:77785447..77792343hg19UCSC Ensembl
Innerchr8:77948002..77954898hg18UCSC Ensembl
Innerchr8:77948002..77954898hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg386897
hg196897
hg186897
hg176897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706108
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522697
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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