A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050051



Internal ID20617091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8386484..8387419hg38UCSC Ensembl
chr19:8451368..8452303hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529103
Supporting Variants
Samples
Known GenesRAB11B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer