A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837096



Internal ID16131052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240788..20424722hg38UCSC Ensembl
Innerchr15:20446041..20629975hg19UCSC Ensembl
Innerchr15:18706055..18889989hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38183935
hg19183935
hg18183935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567306
Supporting Variants
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837096
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