A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578840



Internal ID20951911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33240680..33241163hg38UCSC Ensembl
chr15:33532881..33533364hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239515
Samples
Known GenesTMCO5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578840
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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