A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777138



Internal ID16071094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62362159..62379117hg38UCSC Ensembl
Innerchr11:62129631..62146589hg19UCSC Ensembl
Innerchr11:61886207..61903165hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3816959
hg1916959
hg1816959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555172
Supporting Variants
Samples
Known GenesASRGL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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