A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442159



Internal ID220600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187845370..187845437hg38UCSC Ensembl
chr3:187563158..187563225hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442159
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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