A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779647



Internal ID16073603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82127167..82308588hg38UCSC Ensembl
Innerchr11:81838209..82019630hg19UCSC Ensembl
Innerchr11:81515857..81697278hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38181422
hg19181422
hg18181422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555565
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)nssv779647
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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