A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498672



Internal ID275659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97766677..97771190hg38UCSC Ensembl
chr14:98233014..98237527hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384514
hg194514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498672
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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