A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522182



Internal ID15449475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66791608..66848428hg38UCSC Ensembl
Innerchr6:67501501..67558321hg19UCSC Ensembl
Innerchr6:67558222..67615042hg18UCSC Ensembl
Innerchr6:67558222..67615042hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3856821
hg1956821
hg1856821
hg1756821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694955
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522182
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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