A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526189



Internal ID20899550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54240351..54337012hg38UCSC Ensembl
chr19:54744227..54848283hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3896662
hg19104057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3721n223
Supporting Variantsnssv18200260
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRA6, LILRB2, LILRB5, MIR4752
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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