A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740959



Internal ID20516936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35976912..35976986hg38UCSC Ensembl
chr5:35977014..35977088hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278997
Samples
Known GenesUGT3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740959
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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