A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453737



Internal ID231850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105352932..105357679hg38UCSC Ensembl
chr3:105071776..105076523hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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