A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730678



Internal ID154344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7620221..7624355hg38UCSC Ensembl
chr20:7600868..7605002hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg384135
hg194135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730678
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.034384


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