A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579368



Internal ID20952439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50200140..50201601hg38UCSC Ensembl
chr12:50593923..50595384hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381462
hg191462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233616
Samples
Known GenesLIMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579368
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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