A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583038



Internal ID20956109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58992893..58994235hg38UCSC Ensembl
chr15:59285092..59286434hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241188
Samples
Known GenesRNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583038
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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