A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556463



Internal ID15997186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118061915..118099611hg38UCSC Ensembl
Innerchr11:117932630..117970326hg19UCSC Ensembl
Innerchr11:117437840..117475536hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837697
hg1937697
hg1837697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784610
Samples
Known GenesTMPRSS4, TMPRSS4-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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