A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567433



Internal ID16354842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381928..20418203hg38UCSC Ensembl
Innerchr15:20587181..20623456hg19UCSC Ensembl
Innerchr15:18847195..18883470hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3836276
hg1936276
hg1836276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4198n54
Supporting Variantsnssv837260
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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