A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778756



Internal ID16072712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69093190..69103533hg38UCSC Ensembl
Innerchr11:68860658..68871001hg19UCSC Ensembl
Innerchr11:68617234..68627577hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810344
hg1910344
hg1810344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555318
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)nssv778756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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