A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3716n223



Internal ID22806684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54216875..54667998hg38UCSC Ensembl
chr19:54720744..55179449hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38451124
hg19458706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6599302, nsv6595736
Samples
Known GenesCDC42EP5, KIR3DX1, LAIR1, LAIR2, LENG8, LENG9, LILRA1, LILRA2, LILRA3, LILRA4, LILRA5, LILRA6, LILRB1, LILRB2, LILRB3, LILRB4, LILRB5, MIR4752, MIR8061, TTYH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3716n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer