A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559238



Internal ID20932309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90239873..90743584hg38UCSC Ensembl
chr9:93002155..93505866hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38503712
hg19503712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281384
Samples
Known GenesDIRAS2, LOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559238
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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