A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553089



Internal ID16340498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2388869..2402590hg38UCSC Ensembl
Innerchr11:2410099..2423820hg19UCSC Ensembl
Innerchr11:2366675..2380396hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813722
hg1913722
hg1813722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764511, nssv764510
Samples
Known GenesCD81, TSSC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553089
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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