A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567702



Internal ID20940773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75115405..75116115hg38UCSC Ensembl
chr9:77730321..77731031hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280989
Samples
Known GenesOSTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567702
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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