A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529756



Internal ID305764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60133731..60146471hg38UCSC Ensembl
chr20:58708787..58721527hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812741
hg1912741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733409
Samples
Known GenesLOC284757
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529756
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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