A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564081



Internal ID16351490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25954273..26009405hg38UCSC Ensembl
Innerchr14:26423479..26478611hg19UCSC Ensembl
Innerchr14:25493319..25548451hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3855133
hg1955133
hg1855133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3585n54
Supporting Variantsnssv1149477
SamplesHGDP00734
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564081
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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