A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738882



Internal ID20514853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89010259..89012975hg38UCSC Ensembl
chr1:89475942..89478658hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382717
hg192717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277842
Samples
Known GenesGBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738882
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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