A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088754



Internal ID21997987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58129774..58129774hg38UCSC Ensembl
chr16:58163678..58163678hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088754
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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