A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4268n223



Internal ID22807236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206796501..206805300hg38UCSC Ensembl
chr2:207661225..207670024hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6354339, nsv6336553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4268n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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