A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567421



Internal ID16354830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380065..20418791hg38UCSC Ensembl
Innerchr15:20585318..20624044hg19UCSC Ensembl
Innerchr15:18845332..18884058hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3838727
hg1938727
hg1838727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4205n54
Supporting Variantsnssv837245
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567421
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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