A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510084



Internal ID286714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52141941..52145249hg38UCSC Ensembl
chr14:52608659..52611967hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg383309
hg193309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510084
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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