A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139253



Internal ID338437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148128705..148135220hg38UCSC Ensembl
chr3:147846492..147853007hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386516
hg196516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139253
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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