A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967080



Internal ID22742015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38212101..38212101hg38UCSC Ensembl
chr3:38253592..38253592hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411502
Samples
Known GenesOXSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967080
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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