A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764668



Internal ID20540528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128695772..128695772hg38UCSC Ensembl
chr8:129708018..129708018hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764668
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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