A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267833



Internal ID20834873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110420437..110426643hg38UCSC Ensembl
chr6:110741640..110747846hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386207
hg196207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570600
Supporting Variants
Samples
Known GenesSLC22A16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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