A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289446



Internal ID20498664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64318380..64327849hg38UCSC Ensembl
chr20:62949733..62959202hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389470
hg199470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289446
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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