A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519133



Internal ID15446426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:138149495..138153116hg38UCSC Ensembl
Innerchr6:138470632..138474253hg19UCSC Ensembl
Innerchr6:138512325..138515946hg18UCSC Ensembl
Innerchr6:138512325..138515946hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg383622
hg193622
hg183622
hg173622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694070
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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