A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499257



Internal ID276232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106828695..106883254hg38UCSC Ensembl
chr14:107236923..107289540hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3854560
hg1952618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499257
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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