A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246632



Internal ID20813672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49701349..49703522hg38UCSC Ensembl
chr19:50204606..50206779hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382174
hg192174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596767
Supporting Variants
Samples
Known GenesCPT1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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