A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442094



Internal ID220535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114728452..114735267hg38UCSC Ensembl
chr3:114447299..114454114hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg386816
hg196816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936430
Samples
Known GenesZBTB20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442094
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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