A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv49n206



Internal ID22755353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42067000..42632385hg38UCSC Ensembl
chr10:42596688..43127833hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38565386
hg19531146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5489087, nsv5488943
Samples
Known GenesCCNYL2, LINC00839, LOC441666, ZNF33B, ZNF37BP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv49n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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