A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763494



Internal ID20539354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33462145..33462145hg38UCSC Ensembl
chr8:33319663..33319663hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284887
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763494
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