A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588756



Internal ID20961827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92210767..92211854hg38UCSC Ensembl
chr10:93970524..93971611hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219172
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588756
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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