A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764479



Internal ID15711749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2011014..2036417hg38UCSC Ensembl
Innerchr11:2032244..2057647hg19UCSC Ensembl
Innerchr11:1988820..2014223hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3825404
hg1925404
hg1825404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553065
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)nssv764479
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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