A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732248



Internal ID155914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37123129..37124714hg38UCSC Ensembl
chr20:35751532..35753117hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381586
hg191586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518550
Supporting Variants
Samples
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732248
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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