A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526921



Internal ID15107528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71180534..71240539hg38UCSC Ensembl
Innerchr6:71890237..71950242hg19UCSC Ensembl
Innerchr6:71946958..72006963hg18UCSC Ensembl
Innerchr6:71946958..72006963hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3860006
hg1960006
hg1860006
hg1760006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703285
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526921
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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