A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv316n223



Internal ID22803284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115059845..115069337hg38UCSC Ensembl
chr1:115602466..115611958hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg389493
hg199493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6537300, nsv6549207
Samples
Known GenesTSPAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv316n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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