A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378859



Internal ID22436729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34725310..34747211hg38UCSC Ensembl
chr14:35194516..35216417hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821902
hg1921902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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