A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766317



Internal ID16060273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6095546..6100202hg38UCSC Ensembl
Innerchr11:6116776..6121432hg19UCSC Ensembl
Innerchr11:6073352..6078008hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384657
hg194657
hg184657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553363
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)nssv766317
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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