A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726001



Internal ID149667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43463011..43463120hg38UCSC Ensembl
chr20:42091651..42091760hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525714
Supporting Variants
Samples
Known GenesSRSF6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726001
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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