A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488052



Internal ID21145605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69862619..69867932hg38UCSC Ensembl
chr14:70329336..70334649hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg385314
hg195314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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