A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248448



Internal ID20815488
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 StatusS
Merged Variantsnsv6599302
Supporting Variants
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)nssv18248448
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0006


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