A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567436



Internal ID16354845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381928..20420026hg38UCSC Ensembl
Innerchr15:20587181..20625279hg19UCSC Ensembl
Innerchr15:18847195..18885293hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3838099
hg1938099
hg1838099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4198n54
Supporting Variantsnssv837264
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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