A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272087



Internal ID20839127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75370601..75372299hg38UCSC Ensembl
chr6:76080317..76082015hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381699
hg191699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574099
Supporting Variants
Samples
Known GenesFILIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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