A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591378



Internal ID20964449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22385028..22387052hg38UCSC Ensembl
chr18:19964991..19967015hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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