A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439201



Internal ID217742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39538397..39554732hg38UCSC Ensembl
chr3:39579888..39596223hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3816336
hg1916336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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