A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027889



Internal ID21937232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79392017..79392138hg38UCSC Ensembl
chr13:79966152..79966273hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614429
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027889
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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