A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452444



Internal ID230597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105275627..105276282hg38UCSC Ensembl
chr3:104994471..104995126hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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