A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843967



Internal ID15791237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64700971..64702760hg38UCSC Ensembl
Innerchr15:64993170..64994959hg19UCSC Ensembl
Innerchr15:62780223..62782012hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381790
hg191790
hg181790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569701
Supporting Variants
Samples
Known GenesOAZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843967
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