A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414438



Internal ID193722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33148847..33150987hg38UCSC Ensembl
chr1:33614448..33616588hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382141
hg192141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901390
Samples
Known GenesTRIM62
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414438
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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