A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079593



Internal ID21988826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:60992059..60992059hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079593
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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