A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556523



Internal ID15997246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125209547..125212325hg38UCSC Ensembl
Innerchr11:125079443..125082221hg19UCSC Ensembl
Innerchr11:124584653..124587431hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382779
hg192779
hg182779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784705
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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