A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567338



Internal ID16354747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20352819..20912721hg38UCSC Ensembl
Innerchr15:20558072..21118050hg19UCSC Ensembl
Innerchr15:18818086..19382675hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38559903
hg19559979
hg18564590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4183n54
Supporting Variantsnssv837135
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567338
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