A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992151



Internal ID21901494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17704705..17705206hg38UCSC Ensembl
chr3:17746197..17746698hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538072
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992151
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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