A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564511



Internal ID16351920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41141953..41203992hg38UCSC Ensembl
Innerchr14:41611156..41673195hg19UCSC Ensembl
Innerchr14:40680906..40742945hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3862040
hg1962040
hg1862040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv827067, nssv827068
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564511
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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