A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028413



Internal ID21937756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59762605..60326475hg38UCSC Ensembl
chr16:59796509..60360379hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38563871
hg19563871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028413
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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