A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732648



Internal ID20508572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18675732..18676069hg38UCSC Ensembl
chr20:18656376..18656713hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270148
Samples
Known GenesDTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732648
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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