A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578784



Internal ID20951855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99309782..99310168hg38UCSC Ensembl
chr13:99962036..99962422hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1979n223
Supporting Variantsnssv18235422
Samples
Known GenesMIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer