A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267841



Internal ID20834881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110602607..110603577hg38UCSC Ensembl
chr6:110923810..110924780hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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