A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597089



Internal ID20970160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19378213..19379049hg38UCSC Ensembl
chr19:19489022..19489858hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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