A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586594



Internal ID20959665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37977651..37979053hg38UCSC Ensembl
chr13:38551788..38553190hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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