A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766243



Internal ID16060199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5767103..5787123hg38UCSC Ensembl
Innerchr11:5788333..5808353hg19UCSC Ensembl
Innerchr11:5744909..5764929hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3820021
hg1920021
hg1820021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553334
Supporting Variants
Samples
Known GenesOR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv766243
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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