A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779846



Internal ID16073802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83085381..83125337hg38UCSC Ensembl
Innerchr11:82796423..82836379hg19UCSC Ensembl
Innerchr11:82474071..82514027hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3839957
hg1939957
hg1839957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555604
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)nssv779846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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