A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521916



Internal ID15449209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26463973..26583784hg38UCSC Ensembl
Innerchr11:26485520..26605331hg19UCSC Ensembl
Innerchr11:26442096..26561907hg18UCSC Ensembl
Innerchr11:26442096..26561907hg17UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38119812
hg19119812
hg18119812
hg17119812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694687
Samples
Known GenesANO3, MUC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521916
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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