A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564846



Internal ID16352255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:54230021..54245667hg38UCSC Ensembl
Innerchr14:54696739..54712385hg19UCSC Ensembl
Innerchr14:53766489..53782135hg18UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3815647
hg1915647
hg1815647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3715n54
Supporting Variantsnssv827890
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564846
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