A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766322



Internal ID16060278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6095546..6104430hg38UCSC Ensembl
Innerchr11:6116776..6125660hg19UCSC Ensembl
Innerchr11:6073352..6082236hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388885
hg198885
hg188885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553366
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)nssv766322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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