A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774763



Internal ID16068719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55205378hg38UCSC Ensembl
Innerchr11:54695707..54972854hg19UCSC Ensembl
Innerchr11:54452283..54729430hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38277147
hg19277148
hg18277148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554614
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)nssv774763
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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