A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778764



Internal ID16072720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70132159..70137339hg38UCSC Ensembl
Innerchr11:69978265..69983445hg19UCSC Ensembl
Innerchr11:69655913..69661093hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385181
hg195181
hg185181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555331
Supporting Variants
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778764
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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