A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490048



Internal ID21147601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79355732..79356931hg38UCSC Ensembl
chr13:79929867..79931066hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190231
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490048
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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