A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv782008



Internal ID15729278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102321843..102331284hg38UCSC Ensembl
Innerchr11:102192574..102202015hg19UCSC Ensembl
Innerchr11:101697784..101707225hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg389442
hg199442
hg189442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556142
Supporting Variants
Samples
Known GenesBIRC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv782008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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