A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022288



Internal ID21931631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34693873..34695660hg38UCSC Ensembl
chr14:35163079..35164866hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381788
hg191788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022288
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