A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936360



Internal ID22711713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54219897..54239640hg38UCSC Ensembl
chr19:54723766..54743516hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819744
hg1919751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405363
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936360
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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