A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752919



Internal ID20528779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38212117..38212117hg38UCSC Ensembl
chr3:38253608..38253608hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg384753
hg194753
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289321
Samples
Known GenesOXSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752919
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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