A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411388



Internal ID21068941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158766992..158767289hg38UCSC Ensembl
chr5:158194000..158194297hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126847
Samples
Known GenesEBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411388
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