A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450671



Internal ID228871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43445996..43455687hg38UCSC Ensembl
chr3:43487488..43497179hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389692
hg199692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932321
Samples
Known GenesANO10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450671
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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