A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438158



Internal ID216727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41028458..41031827hg38UCSC Ensembl
chr3:41069949..41073318hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383370
hg193370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438158
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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