A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598303



Internal ID20971374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37615087..37616177hg38UCSC Ensembl
chr19:38105988..38107078hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3505n223
Supporting Variantsnssv18248333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598303
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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