A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588582



Internal ID20961653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131294422..131666124hg38UCSC Ensembl
chr12:131778967..132150669hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38371703
hg19371703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1742n223
Supporting Variantsnssv18223234
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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