A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524782



Internal ID20898143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14690835..14695921hg38UCSC Ensembl
chr19:14801647..14806733hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385087
hg195087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197410
Samples
Known GenesZNF333
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524782
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