A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561345



Internal ID20934416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83990271..83991022hg38UCSC Ensembl
chr9:86605186..86605937hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281237
Samples
Known GenesRMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561345
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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