A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591460



Internal ID20964531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95282082..95282614hg38UCSC Ensembl
chr13:95934336..95934868hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1973n223
Supporting Variantsnssv18227030
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591460
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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