A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039863



Internal ID21949206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58232843..58232896hg38UCSC Ensembl
chr16:58266747..58266800hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039863
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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