A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027400



Internal ID21936743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62288999..62305467hg38UCSC Ensembl
chr16:62322903..62339371hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3816469
hg1916469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027400
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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