A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943211



Internal ID22718656
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 StatusM
Merged Variants
Supporting Variantsnssv17378859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943211
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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