A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938935



Internal ID22714321
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 StatusM
Merged Variants
Supporting Variantsnssv17386102
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938935
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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