A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567241



Internal ID16354650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20189043..20407587hg38UCSC Ensembl
Innerchr15:20394296..20612840hg19UCSC Ensembl
Innerchr15:18654310..18872854hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38218545
hg19218545
hg18218545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4178n54
Supporting Variantsnssv836994
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567241
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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