A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753462



Internal ID21391860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54220823..54240190hg38UCSC Ensembl
chr19:54724693..54744066hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819368
hg1919374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432858
Supporting Variants
SamplesSMI018
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753462
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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