A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv377n172



Internal ID22814751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54220029..54240190hg38UCSC Ensembl
chr19:54723893..54744066hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3820162
hg1920174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432858, nsv4432857
SamplesSMI034, SMI018
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv377n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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