A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520020



Internal ID20893381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48433016..48438518hg38UCSC Ensembl
chr19:48936273..48941775hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385503
hg195503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048390
Samples
Known GenesGRIN2D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520020
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