A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594687



Internal ID20967758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9403176..9570594hg38UCSC Ensembl
chr12:9555772..9723190hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38167419
hg19167419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1395n223
Supporting Variantsnssv18236930
Samples
Known GenesDDX12P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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