A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038746



Internal ID21948089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98017670..98179928hg38UCSC Ensembl
chr13:98669924..98832182hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38162259
hg19162259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616717
Samples
Known GenesFARP1, IPO5, RNF113B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038746
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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