A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443592



Internal ID221986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46462160..46462330hg38UCSC Ensembl
chr3:46503650..46503820hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933306
Samples
Known GenesLTF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443592
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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