A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522535



Internal ID15449828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129792047..129832154hg38UCSC Ensembl
Innerchr8:130804293..130844400hg19UCSC Ensembl
Innerchr8:130873475..130913582hg18UCSC Ensembl
Innerchr8:130873475..130913582hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3840108
hg1940108
hg1840108
hg1740108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705909
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522535
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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