A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593691



Internal ID20966762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112253131..112277124hg38UCSC Ensembl
chr10:114012889..114036882hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3823994
hg1923994
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593691
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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