A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766939



Internal ID15714209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7664234..7665353hg38UCSC Ensembl
Innerchr11:7685465..7686584hg19UCSC Ensembl
Innerchr11:7642041..7643160hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381120
hg191120
hg181120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553407
Supporting Variants
Samples
Known GenesCYB5R2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv766939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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