A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730647



Internal ID20506559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:393030..393116hg38UCSC Ensembl
chr20:373674..373760hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274530
Samples
Known GenesTRIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730647
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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