A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546789



Internal ID320699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52313728..52313779hg38UCSC Ensembl
chr14:52780446..52780497hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546789
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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