A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567240



Internal ID16354649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20189043..20396902hg38UCSC Ensembl
Innerchr15:20394296..20602155hg19UCSC Ensembl
Innerchr15:18654310..18862169hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38207860
hg19207860
hg18207860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4178n54
Supporting Variantsnssv836993
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567240
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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