A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593099



Internal ID20966170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41236275..41237181hg38UCSC Ensembl
chr13:41810411..41811317hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1811n223
Supporting Variantsnssv18226099
Samples
Known GenesMTRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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