A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747813



Internal ID20523834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26078267..26078430hg38UCSC Ensembl
chr8:25935783..25935946hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747813
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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