A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450043



Internal ID228262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151623807..151628026hg38UCSC Ensembl
chr3:151341595..151345814hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384220
hg194220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450043
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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