A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743394



Internal ID20519382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128642765..128642831hg38UCSC Ensembl
chr8:129655011..129655077hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743394
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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