A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725959



Internal ID149625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40586218..40586341hg38UCSC Ensembl
chr20:39214858..39214981hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725959
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01561


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