A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104646



Internal ID22013879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89460824..90479383hg38UCSC Ensembl
chr3:89509974..90504854hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg381018560
hg19994881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550810
Samples
Known GenesEPHA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104646
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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