A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027991



Internal ID21937334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47019913..47031654hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3811742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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