A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567306



Internal ID16354715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240788..20424722hg38UCSC Ensembl
Innerchr15:20446041..20629975hg19UCSC Ensembl
Innerchr15:18706055..18889989hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38183935
hg19183935
hg18183935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4179n54
Supporting Variantsnssv837096
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567306
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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