A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732749



Internal ID156415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47619875..47620183hg38UCSC Ensembl
chr20:46248619..46248927hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529739
Supporting Variants
Samples
Known GenesNCOA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732749
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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