A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553767



Internal ID16341176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23759988..23923113hg38UCSC Ensembl
Innerchr11:23781534..23944659hg19UCSC Ensembl
Innerchr11:23738110..23901235hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38163126
hg19163126
hg18163126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768964
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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