A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092020



Internal ID22001253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50932058..50932058hg38UCSC Ensembl
chr13:51506194..51506194hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601356
Samples
Known GenesRNASEH2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092020
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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