A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991173



Internal ID21900516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101562005..101564769hg38UCSC Ensembl
chr3:101280849..101283613hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg382765
hg192765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544858
Samples
Known GenesTRMT10C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991173
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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