A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440493



Internal ID218997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163606907..163644743hg38UCSC Ensembl
chr3:163324695..163362531hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3837837
hg1937837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440493
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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