A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980740



Internal ID21890083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111543640..111543722hg38UCSC Ensembl
chr1:112086262..112086344hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518959
Samples
Known GenesADORA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980740
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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