A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534626



Internal ID20907987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:606698..611991hg38UCSC Ensembl
chr19:606698..611991hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385294
hg195294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198975
Samples
Known GenesHCN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534626
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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