A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592809



Internal ID20965880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110728079..110728597hg38UCSC Ensembl
chr13:111380426..111380944hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1996n223
Supporting Variantsnssv18235604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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