A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591639



Internal ID20964710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32540143..32541165hg38UCSC Ensembl
chr13:33114280..33115302hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1795n223
Supporting Variantsnssv18230243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591639
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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