A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580302



Internal ID20953373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59629708..59631966hg38UCSC Ensembl
chr17:57707069..57709327hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg382259
hg192259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243774
Samples
Known GenesCLTC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580302
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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