A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579132



Internal ID20952203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73491181..73491781hg38UCSC Ensembl
chr10:75250939..75251539hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv808n223
Supporting Variantsnssv18235413
Samples
Known GenesPPP3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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