A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784711



Internal ID15731981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126405064..126426694hg38UCSC Ensembl
Innerchr11:126274959..126296589hg19UCSC Ensembl
Innerchr11:125780169..125801799hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3821631
hg1921631
hg1821631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556531
Supporting Variants
Samples
Known GenesKIRREL3, ST3GAL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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