A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733294



Internal ID156960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57392778..57393227hg38UCSC Ensembl
chr20:55967834..55968283hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532550
Supporting Variants
Samples
Known GenesMIR5095, RBM38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733294
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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