A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588979



Internal ID20962050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22903802..22905799hg38UCSC Ensembl
chr18:20483765..20485762hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381998
hg191998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3327n223
Supporting Variantsnssv18246131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588979
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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