A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079232



Internal ID21988465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112955148..112955148hg38UCSC Ensembl
chr5:112290845..112290845hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079232
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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