A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528827



Internal ID20902188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38935671..38941712hg38UCSC Ensembl
chr19:39426311..39432352hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386042
hg196042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047828
Samples
Known GenesFBXO17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528827
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