A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583754



Internal ID20956825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86362364..87188213hg38UCSC Ensembl
chr13:87014619..87840468hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38825850
hg19825850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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