A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437038



Internal ID215639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32470086..32470197hg38UCSC Ensembl
chr3:32511578..32511689hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437038
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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