A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590807



Internal ID20963878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39301450..39302439hg38UCSC Ensembl
chr17:37457703..37458692hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38990
hg19990
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242900
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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