A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739680



Internal ID20515655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97420421..97425992hg38UCSC Ensembl
chr1:97885977..97891548hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg385572
hg195572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275533
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739680
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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