A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580898



Internal ID20953969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65148990..65150468hg38UCSC Ensembl
chr17:63145108..63146586hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243315
Samples
Known GenesRGS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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