A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523826



Internal ID15104433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137874929..137876194hg38UCSC Ensembl
Innerchr6:138196066..138197331hg19UCSC Ensembl
Innerchr6:138237759..138239024hg18UCSC Ensembl
Innerchr6:138237759..138239024hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381266
hg191266
hg181266
hg171266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699657
Samples
Known GenesTNFAIP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523826
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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