A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526998



Internal ID15454291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4933377..5053071hg38UCSC Ensembl
Innerchr11:4954607..5074301hg19UCSC Ensembl
Innerchr11:4911183..5030877hg18UCSC Ensembl
Innerchr11:4911183..5030877hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38119695
hg19119695
hg18119695
hg17119695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703373
Samples
Known GenesMMP26, OR51A2, OR51A4, OR51L1, OR52J3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526998
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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