A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586259



Internal ID20959330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57247411..57456716hg38UCSC Ensembl
chr15:57539609..57748914hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38209306
hg19209306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241127
Samples
Known GenesCGNL1, LINC00926, TCF12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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