A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567266



Internal ID16354675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20207597..20421165hg38UCSC Ensembl
Innerchr15:20412850..20626418hg19UCSC Ensembl
Innerchr15:18672864..18886432hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38213569
hg19213569
hg18213569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4178n54
Supporting Variantsnssv837029
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567266
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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