A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274811



Internal ID20841851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84595873..85427122hg38UCSC Ensembl
chr6:85305591..86136840hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38831250
hg19831250
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562641
Supporting Variants
Samples
Known GenesTBX18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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