A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630687



Internal ID21822734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30560631..30563190hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059702
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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