A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591874



Internal ID20964945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56043476..56115080hg38UCSC Ensembl
chr13:56617610..56689214hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3871605
hg1971605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591874
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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