A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037765



Internal ID21947108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69227721..69227776hg38UCSC Ensembl
chr14:69694438..69694493hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615331
Samples
Known GenesEXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037765
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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