A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024558



Internal ID21933901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58395928..58396233hg38UCSC Ensembl
chr16:58429832..58430137hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620468
Samples
Known GenesGINS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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