A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730572



Internal ID154238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5582212..5583072hg38UCSC Ensembl
chr20:5562858..5563718hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524821
Supporting Variants
Samples
Known GenesGPCPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730572
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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