A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754339



Internal ID20530199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1799332..1799332hg38UCSC Ensembl
chr8:1747498..1747498hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754339
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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