A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881611



Internal ID22656587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97420421..97425990hg38UCSC Ensembl
chr1:97885977..97891546hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg385570
hg195570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392165
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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