A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562333



Internal ID20935404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83704728..83705392hg38UCSC Ensembl
chr9:86319643..86320307hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281218
Samples
Known GenesUBQLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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