A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv292n223



Internal ID22803260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105413101..105533185hg38UCSC Ensembl
chr1:105955723..106075807hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38120085
hg19120085
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6316099, nsv6326420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv292n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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