A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778609



Internal ID15725879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67627424..67640770hg38UCSC Ensembl
Innerchr11:67394895..67408241hg19UCSC Ensembl
Innerchr11:67151471..67164817hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3813347
hg1913347
hg1813347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555272
Supporting Variants
Samples
Known GenesNUDT8, TBX10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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