A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444372



Internal ID222747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104308059..104364248hg38UCSC Ensembl
chr3:104026903..104083092hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3856190
hg1956190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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