A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039473



Internal ID21948816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63732579..63747423hg38UCSC Ensembl
chr16:63766483..63781327hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3814845
hg1914845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039473
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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