A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271546



Internal ID20838586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75669178..75670139hg38UCSC Ensembl
chr6:76378894..76379855hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570733
Supporting Variants
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271546
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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