A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539367



Internal ID314323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37720446..37720446hg38UCSC Ensembl
chr14:38189651..38189651hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539367
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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