A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752495



Internal ID20528355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128286433..128286433hg38UCSC Ensembl
chr8:129298679..129298679hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752495
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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