A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447776



Internal ID226068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189506718..189507582hg38UCSC Ensembl
chr3:189224507..189225371hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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