A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768951



Internal ID16062907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23238450..23387990hg38UCSC Ensembl
Innerchr11:23259996..23409536hg19UCSC Ensembl
Innerchr11:23216572..23366112hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38149541
hg19149541
hg18149541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553753
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)nssv768951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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