A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524843



Internal ID15452136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121498201..121506695hg38UCSC Ensembl
Innerchr8:122510441..122518935hg19UCSC Ensembl
Innerchr8:122579622..122588116hg18UCSC Ensembl
Innerchr8:122579622..122588116hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg388495
hg198495
hg188495
hg178495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700845
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524843
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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