A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585054



Internal ID20958125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50734279..50735137hg38UCSC Ensembl
chr17:48811640..48812498hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3183n223
Supporting Variantsnssv18245171
Samples
Known GenesLUC7L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585054
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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