A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578999



Internal ID20952070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45312294..45312554hg38UCSC Ensembl
chr13:45886429..45886689hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578999
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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