A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9n206



Internal ID22755313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10009197..10016506hg38UCSC Ensembl
chr1:10069255..10076564hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387310
hg197310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5415321, nsv5426467
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv9n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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