A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv398n223



Internal ID22803366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158991501..159005500hg38UCSC Ensembl
chr1:158961291..158975290hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6331611, nsv6330553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv398n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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