A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267850



Internal ID20834890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110790747..110792050hg38UCSC Ensembl
chr6:111111950..111113253hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572071
Supporting Variants
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267850
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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