A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991989



Internal ID21901332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174833742..174834153hg38UCSC Ensembl
chr3:174551532..174551943hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991989
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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