A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524256



Internal ID20897617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45797385..45798756hg38UCSC Ensembl
chr19:46300643..46302014hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046529
Samples
Known GenesRSPH6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524256
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