A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028475



Internal ID21937818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53539097..53539370hg38UCSC Ensembl
chr16:53573009..53573282hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028475
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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