A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502082



Internal ID278959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97419206..97423511hg38UCSC Ensembl
chr14:97885543..97889848hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384306
hg194306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502082
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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