A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768992



Internal ID16062948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24419419..24431228hg38UCSC Ensembl
Innerchr11:24440965..24452774hg19UCSC Ensembl
Innerchr11:24397541..24409350hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3811810
hg1911810
hg1811810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553796
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)nssv768992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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