A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090739



Internal ID21432489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79392110..79392181hg38UCSC Ensembl
chr13:79966245..79966316hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598043
Supporting Variants
SamplesHG00731
Known GenesRBM26
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090739
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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