A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272098



Internal ID20839138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89101445..89102161hg38UCSC Ensembl
chr6:89811164..89811880hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567207
Supporting Variants
Samples
Known GenesSRSF12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272098
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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