A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434181



Internal ID212863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114291663..114293476hg38UCSC Ensembl
chr3:114010510..114012323hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434181
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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