A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581254



Internal ID20954325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118289738..118290636hg38UCSC Ensembl
chr12:118727543..118728441hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230791
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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