A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993121



Internal ID21902464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36536341..36537822hg38UCSC Ensembl
chr3:36577833..36579314hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381482
hg191482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544907
Samples
Known GenesSTAC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993121
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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