A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738181



Internal ID20514148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63028026..63028549hg38UCSC Ensembl
chr20:61659378..61659901hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288994
Samples
Known GenesLOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738181
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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