A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762630



Internal ID20538490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103909372..103909372hg38UCSC Ensembl
chr10:105669130..105669130hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285537
Samples
Known GenesOBFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762630
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