A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566039



Internal ID16353448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104257096..104335962hg38UCSC Ensembl
Innerchr14:104723433..104802299hg19UCSC Ensembl
Innerchr14:103793186..103873344hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3878867
hg1978867
hg1880159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3950n54
Supporting Variantsnssv1148708, nssv834424
Samples1782681313_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566039
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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