A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364890



Internal ID21022443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19471109..19473871hg38UCSC Ensembl
chr3:19512601..19515363hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382763
hg192763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101256
Samples
Known GenesKCNH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364890
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