A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144036



Internal ID343238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25773675..25781713hg38UCSC Ensembl
chr14:26242881..26250919hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg388039
hg198039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144036
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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