A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080124



Internal ID21989357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113448615..113448615hg38UCSC Ensembl
chr5:112784312..112784312hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540539
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080124
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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