A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591724



Internal ID20964795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103940092..103941077hg38UCSC Ensembl
chr10:105699850..105700835hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591724
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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