A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437558



Internal ID216143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75983679..76765748hg38UCSC Ensembl
chr3:76032830..76814899hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38782070
hg19782070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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