A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565021



Internal ID16352430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221413..70224160hg38UCSC Ensembl
Innerchr14:70688130..70690877hg19UCSC Ensembl
Innerchr14:69757883..69760630hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382748
hg192748
hg182748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3749n54
Supporting Variantsnssv828972, nssv828971
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565021
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