A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589063



Internal ID20962134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110727868..110728598hg38UCSC Ensembl
chr13:111380215..111380945hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1996n223
Supporting Variantsnssv18223683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589063
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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