A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556510



Internal ID15997233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125206408..125209975hg38UCSC Ensembl
Innerchr11:125076304..125079871hg19UCSC Ensembl
Innerchr11:124581514..124585081hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg383568
hg193568
hg183568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784687
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556510
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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