A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574670



Internal ID20947741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81675950..81677364hg38UCSC Ensembl
chr9:84290865..84292279hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281163
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574670
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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