A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779841



Internal ID16073797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82225960..82330731hg38UCSC Ensembl
Innerchr11:81937002..82041773hg19UCSC Ensembl
Innerchr11:81614650..81719421hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38104772
hg19104772
hg18104772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555599
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)nssv779841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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