A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453011



Internal ID231151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155402741..155406987hg38UCSC Ensembl
chr3:155120530..155124776hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384247
hg194247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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