A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411019



Internal ID21068572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90644201..90691800hg38UCSC Ensembl
chr5:89940018..89987617hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3847600
hg1947600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134938
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411019
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