A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579206



Internal ID20952277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117107880..117108284hg38UCSC Ensembl
chr12:117545685..117546089hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579206
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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