A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725968



Internal ID149634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40901771..40908108hg38UCSC Ensembl
chr20:39530411..39536748hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg386338
hg196338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725968
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.016406


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