A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451672



Internal ID229847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18315228..18318385hg38UCSC Ensembl
chr3:18356720..18359877hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383158
hg193158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451672
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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