A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596767



Internal ID20969838
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 StatusM
Merged Variants
Supporting Variantsnssv18246632
Samples
Known GenesCPT1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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