A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268590



Internal ID20835630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117432318..117433224hg38UCSC Ensembl
chr6:117753481..117754387hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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