A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564572



Internal ID16351981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42502585..42614354hg38UCSC Ensembl
Innerchr14:42971788..43083557hg19UCSC Ensembl
Innerchr14:42041538..42153307hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38111770
hg19111770
hg18111770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3671n54
Supporting Variantsnssv827230
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564572
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