A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730633



Internal ID154299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6879348..6879712hg38UCSC Ensembl
chr20:6859995..6860359hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001721


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