A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567200



Internal ID20940271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86794975..86799667hg38UCSC Ensembl
chr9:89409890..89414582hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg384693
hg194693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567200
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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