A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569427



Internal ID16356836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52749690..52799699hg38UCSC Ensembl
Innerchr15:53041887..53091896hg19UCSC Ensembl
Innerchr15:50829179..50879188hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3850010
hg1950010
hg1850010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148867
SamplesNINDS_54
Known GenesONECUT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569427
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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