A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594746



Internal ID20967817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11817659..11825678hg38UCSC Ensembl
chr18:11817658..11825677hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg388020
hg198020
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243425
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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