A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776522



Internal ID15723792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55626700hg38UCSC Ensembl
Innerchr11:55373973..55394176hg19UCSC Ensembl
Innerchr11:55130549..55150752hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3820204
hg1920204
hg1820204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554911
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)nssv776522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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