A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271545



Internal ID20838585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75669040..75670209hg38UCSC Ensembl
chr6:76378756..76379925hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565853
Supporting Variants
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271545
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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