A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936430



Internal ID25012
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 StatusS
Merged Variantsnsv5442094
Supporting Variants
Samples
Known GenesZBTB20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936430
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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