A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621245



Internal ID21813292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49943964..49946500hg38UCSC Ensembl
chr16:49977875..49980411hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg382537
hg192537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621245
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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