A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725930



Internal ID149596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35627992..36077048hg38UCSC Ensembl
chr20:34215914..34664970hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38449057
hg19449057
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557509
Supporting Variants
Samples
Known GenesCNBD2, CPNE1, LINC00657, NFS1, PHF20, RBM12, RBM39, ROMO1, SCAND1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725930
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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