A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274094



Internal ID20841134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73475533..73476379hg38UCSC Ensembl
chr6:74185256..74186102hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569611
Supporting Variants
Samples
Known GenesMTO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274094
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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