A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995082



Internal ID21904425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121921980..121922183hg38UCSC Ensembl
chr4:122843135..122843338hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554201
Samples
Known GenesTRPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995082
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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