A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730474



Internal ID154140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4013743..4019006hg38UCSC Ensembl
chr20:3994390..3999653hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385264
hg195264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528396
Supporting Variants
Samples
Known GenesRNF24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730474
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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