A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732125



Internal ID155791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34777872..34781258hg38UCSC Ensembl
chr20:33365675..33369061hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519762
Supporting Variants
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732125
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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