A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766314



Internal ID16060270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6095064..6099456hg38UCSC Ensembl
Innerchr11:6116294..6120686hg19UCSC Ensembl
Innerchr11:6072870..6077262hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384393
hg194393
hg184393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553360
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)nssv766314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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