A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590981



Internal ID20964052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94640476..94641063hg38UCSC Ensembl
chr12:95034252..95034839hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221840
Samples
Known GenesTMCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590981
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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