A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048874



Internal ID20615914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54221825..54241469hg38UCSC Ensembl
chr19:54725697..54745345hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819645
hg1919649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533908
Supporting Variants
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00019


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