A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072513



Internal ID21981746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111922055..111922055hg38UCSC Ensembl
chr6:112243258..112243258hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382699
hg192699
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072513
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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