A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589130



Internal ID20962201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44839010..45061893hg38UCSC Ensembl
chr15:45131208..45354091hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38222884
hg19222884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2519n223
Supporting Variantsnssv18240271
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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