A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450478



Internal ID228684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191657821..191724423hg38UCSC Ensembl
chr3:191375610..191442212hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3866603
hg1966603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450478
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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