A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732124



Internal ID155790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34772615..34772615hg38UCSC Ensembl
chr20:33360418..33360418hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553684
Supporting Variants
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732124
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003906


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