A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv765573



Internal ID16059529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5698605..5701151hg38UCSC Ensembl
Innerchr11:5719835..5722381hg19UCSC Ensembl
Innerchr11:5676411..5678957hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382547
hg192547
hg182547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553274
Supporting Variants
Samples
Known GenesTRIM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv765573
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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