A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564968



Internal ID16352377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69533682..69554845hg38UCSC Ensembl
Innerchr14:70000399..70021562hg19UCSC Ensembl
Innerchr14:69070152..69091315hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3821164
hg1921164
hg1821164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3737n54
Supporting Variantsnssv828630
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564968
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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