A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579866



Internal ID20952937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105937471..107267814hg38UCSC Ensembl
chr10:107697229..109027572hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381330344
hg191330344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218168
Samples
Known GenesSORCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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