A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564816



Internal ID16352225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48321920..48428035hg38UCSC Ensembl
Innerchr14:48791123..48897238hg19UCSC Ensembl
Innerchr14:47860873..47966988hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38106116
hg19106116
hg18106116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3712n54
Supporting Variantsnssv827845
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564816
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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