A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433289



Internal ID21395291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60058946..60059945hg38UCSC Ensembl
chr20:58634001..58635000hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747441
SamplesMDQ010
Known GenesC20orf197
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433289
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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