A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532192



Internal ID308120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37104478..37106047hg38UCSC Ensembl
chr20:35732881..35734450hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732246
Samples
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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