A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093034



Internal ID22002267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98401415..98401415hg38UCSC Ensembl
chr13:99053669..99053669hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608088
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093034
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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