A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764010



Internal ID20539870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141074105..141074105hg38UCSC Ensembl
chr8:142084204..142084204hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764010
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer