A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1395n223



Internal ID22804363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9403176..9570660hg38UCSC Ensembl
chr12:9555772..9723256hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38167485
hg19167485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6589038, nsv6576286, nsv6594687, nsv6594292
Samples
Known GenesDDX12P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1395n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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