A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519294



Internal ID20892655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33325658..33331874hg38UCSC Ensembl
chr19:33816564..33822780hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg386217
hg196217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519294
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