A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234612



Internal ID20801652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92282508..92283988hg38UCSC Ensembl
chr10:94042265..94043745hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381481
hg191481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585391
Supporting Variants
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234612
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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