A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579593



Internal ID20952664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32196909..32197530hg38UCSC Ensembl
chr17:30523928..30524549hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244419
Samples
Known GenesRHOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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