A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449031



Internal ID227280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5757911..5765891hg38UCSC Ensembl
chr3:5799598..5807578hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg387981
hg197981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449031
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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