A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760099



Internal ID20535959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54282297..54627696hg38UCSC Ensembl
chr19:54786152..55139147hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38345400
hg19352996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269511
Samples
Known GenesCDC42EP5, KIR3DX1, LAIR1, LAIR2, LENG8, LENG9, LILRA1, LILRA2, LILRA3, LILRA4, LILRA5, LILRB1, TTYH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760099
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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