A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526061



Internal ID15106668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25708486..25725253hg38UCSC Ensembl
Innerchr6:25708714..25725481hg19UCSC Ensembl
Innerchr6:25816693..25833460hg18UCSC Ensembl
Innerchr6:25816693..25833460hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3816768
hg1916768
hg1816768
hg1716768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702299
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526061
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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