A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593030



Internal ID20966101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115551323..115552917hg38UCSC Ensembl
chr12:115989128..115990722hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg381595
hg191595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593030
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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