A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843926



Internal ID16137882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414365..62428164hg38UCSC Ensembl
Innerchr15:62706564..62720363hg19UCSC Ensembl
Innerchr15:60493856..60507655hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813800
hg1913800
hg1813800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569683
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843926
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