A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526053



Internal ID15453346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75146391..75150500hg38UCSC Ensembl
Innerchr11:74857436..74861545hg19UCSC Ensembl
Innerchr11:74535084..74539193hg18UCSC Ensembl
Innerchr11:74535084..74539193hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384110
hg194110
hg184110
hg174110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702290
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526053
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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