A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv770388



Internal ID16064344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29466724..29703240hg38UCSC Ensembl
Innerchr11:29488271..29724787hg19UCSC Ensembl
Innerchr11:29444847..29681363hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38236517
hg19236517
hg18236517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553941
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv770388
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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