A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567267



Internal ID16354676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20207597..20424904hg38UCSC Ensembl
Innerchr15:20412850..20630157hg19UCSC Ensembl
Innerchr15:18672864..18890171hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38217308
hg19217308
hg18217308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4178n54
Supporting Variantsnssv837031, nssv837032, nssv837030, nssv837033
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567267
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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