A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784657



Internal ID15731927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125205679..125213220hg38UCSC Ensembl
Innerchr11:125075575..125083116hg19UCSC Ensembl
Innerchr11:124580785..124588326hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387542
hg197542
hg187542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556494
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)nssv784657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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