A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267783



Internal ID20834823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108297287..108299267hg38UCSC Ensembl
chr6:108618491..108620471hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567666
Supporting Variants
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267783
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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