A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5545269



Internal ID319324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31704027..31704077hg38UCSC Ensembl
chr3:31745519..31745569hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932161
Samples
Known GenesOSBPL10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5545269
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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