A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614429



Internal ID21806476
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 StatusS
Merged Variantsnsv6027889
Supporting Variants
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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