A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578776



Internal ID20951847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24503709..24504343hg38UCSC Ensembl
chr18:22083673..22084307hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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