A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319179



Internal ID20852271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97401901..97403400hg38UCSC Ensembl
chr1:97867457..97868956hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065679
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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