A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048872



Internal ID20615912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54221139..54278869hg38UCSC Ensembl
chr19:54725048..54782724hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3857731
hg1957677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522907
Supporting Variants
Samples
Known GenesLILRA6, LILRB2, LILRB3, LILRB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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