A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438380



Internal ID216946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44914372..44915704hg38UCSC Ensembl
chr3:44955864..44957196hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933674
Samples
Known GenesTGM4, ZDHHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438380
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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