A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567286



Internal ID16354695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20217246..20426741hg38UCSC Ensembl
Innerchr15:20422499..20631994hg19UCSC Ensembl
Innerchr15:18682513..18892008hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38209496
hg19209496
hg18209496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4178n54
Supporting Variantsnssv837062, nssv837064, nssv837061, nssv837063
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567286
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer