A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567439



Internal ID16354848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20382975..20419601hg38UCSC Ensembl
Innerchr15:20588228..20624854hg19UCSC Ensembl
Innerchr15:18848242..18884868hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3836627
hg1936627
hg1836627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4198n54
Supporting Variantsnssv837267
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567439
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