A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564621



Internal ID16352030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42832113..42885658hg38UCSC Ensembl
Innerchr14:43301316..43354861hg19UCSC Ensembl
Innerchr14:42371066..42424611hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3853546
hg1953546
hg1853546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3680n54
Supporting Variantsnssv827505, nssv827506
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564621
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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