A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv399n223



Internal ID22803367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159043301..159048622hg38UCSC Ensembl
chr1:159013091..159018412hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg385322
hg195322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6326222, nsv6315833
Samples
Known GenesIFI16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv399n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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