A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270914



Internal ID20837954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25964830..25965920hg38UCSC Ensembl
chr6:25965058..25966148hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573571
Supporting Variants
Samples
Known GenesTRIM38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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