A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597661



Internal ID20970732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70342029..70342443hg38UCSC Ensembl
chr18:68009265..68009679hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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