A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271568



Internal ID20838608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75858397..75859419hg38UCSC Ensembl
chr6:76568114..76569136hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559856
Supporting Variants
Samples
Known GenesMYO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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