A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832699



Internal ID15779969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93990701..94031622hg38UCSC Ensembl
Innerchr14:94457047..94497968hg19UCSC Ensembl
Innerchr14:93526800..93567721hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3840922
hg1940922
hg1840922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565620
Supporting Variants
Samples
Known GenesLINC00521, OTUB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832699
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