A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599302



Internal ID20972373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54216875..54667837hg38UCSC Ensembl
chr19:54720744..55179288hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38450963
hg19458545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3716n223
Supporting Variantsnssv18248448
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)nsv6599302
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