A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590544



Internal ID20963615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33341413..33341986hg38UCSC Ensembl
chr13:33915550..33916123hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1797n223
Supporting Variantsnssv18225752
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590544
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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