A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567189



Internal ID16354598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20051457..20761858hg38UCSC Ensembl
Innerchr15:20256710..20967187hg19UCSC Ensembl
Innerchr15:18516724..19227219hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38710402
hg19710478
hg18710496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4174n54
Supporting Variantsnssv836928
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567189
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