A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273211



Internal ID20840251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147056892..147059804hg38UCSC Ensembl
chr6:147378028..147380940hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567627
Supporting Variants
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273211
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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