A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578824



Internal ID20951895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49758902..49760376hg38UCSC Ensembl
chr18:47285272..47286746hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg381475
hg191475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578824
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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