A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020300



Internal ID21929643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110747801..110747868hg38UCSC Ensembl
chr10:112507559..112507626hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579495
Samples
Known GenesRBM20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020300
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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