A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564145



Internal ID16351554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27989467..28049942hg38UCSC Ensembl
Innerchr14:28458673..28519148hg19UCSC Ensembl
Innerchr14:27528513..27589002hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3860476
hg1960476
hg1860490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3598n54
Supporting Variantsnssv825083
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer