A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv773986



Internal ID16067942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50372893..50807137hg38UCSC Ensembl
Innerchr11:50332064..50766308hg19UCSC Ensembl
Innerchr11:50288640..50722884hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38434245
hg19434245
hg18434245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554409
Supporting Variants
Samples
Known GenesLOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv773986
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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