A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506141



Internal ID282896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74103525..74131413hg38UCSC Ensembl
chr14:74570228..74598116hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827889
hg1927889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699268
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506141
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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