A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269962



Internal ID20837002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167785415..167785884hg38UCSC Ensembl
chr6:168186095..168186564hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565383
Supporting Variants
Samples
Known GenesC6orf123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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