A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784689



Internal ID15731959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125206408..125211544hg38UCSC Ensembl
Innerchr11:125076304..125081440hg19UCSC Ensembl
Innerchr11:124581514..124586650hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385137
hg195137
hg185137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556512
Supporting Variants
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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