A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894564



Internal ID22669637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113157755..113175000hg38UCSC Ensembl
chr3:112876602..112893847hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3817246
hg1917246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894564
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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