A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567336



Internal ID16354745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20352819..20424904hg38UCSC Ensembl
Innerchr15:20558072..20630157hg19UCSC Ensembl
Innerchr15:18818086..18890171hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3872086
hg1972086
hg1872086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n54
Supporting Variantsnssv837133
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer