A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273299



Internal ID20840339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28831504..29349940hg38UCSC Ensembl
chr6:28799281..29317717hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38518437
hg19518437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564524
Supporting Variants
Samples
Known GenesC6orf100, HCG14, LOC100129636, LOC401242, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, TRIM27, ZNF311
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00063


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