A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596082



Internal ID20969153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16640154..16640989hg38UCSC Ensembl
chr19:16750965..16751800hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596082
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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