A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768864



Internal ID16062820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21838458..22134911hg38UCSC Ensembl
Innerchr11:21860004..22156457hg19UCSC Ensembl
Innerchr11:21816580..22113033hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38296454
hg19296454
hg18296454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553725
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)nssv768864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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