A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556509



Internal ID15997232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125206261..125215292hg38UCSC Ensembl
Innerchr11:125076157..125085188hg19UCSC Ensembl
Innerchr11:124581367..124590398hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg389032
hg199032
hg189032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2190n54
Supporting Variantsnssv784686, nssv784685
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556509
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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