A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578596



Internal ID20951667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60356327..60358016hg38UCSC Ensembl
chr13:60930461..60932150hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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