A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv765902



Internal ID16059858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5755980..5781122hg38UCSC Ensembl
Innerchr11:5777210..5802352hg19UCSC Ensembl
Innerchr11:5733786..5758928hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825143
hg1925143
hg1825143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553308
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)nssv765902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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