A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837103



Internal ID16131059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20242941..22111284hg38UCSC Ensembl
Innerchr15:20448194..22399235hg19UCSC Ensembl
Innerchr15:18708208..19900599hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381868344
hg191951042
hg181192392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567310
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837103
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