A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146802



Internal ID346007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54221400..54337000hg38UCSC Ensembl
chr19:54725272..54848271hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38115601
hg19123000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725507
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRA6, LILRB2, LILRB3, LILRB5, MIR4752
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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