A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv769275



Internal ID16063231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26772821..26842068hg38UCSC Ensembl
Innerchr11:26794368..26863615hg19UCSC Ensembl
Innerchr11:26750944..26820191hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3869248
hg1969248
hg1869248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553910
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)nssv769275
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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