A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1282n145



Internal ID22814298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139929033..139934291hg38UCSC Ensembl
chrX:139011192..139016450hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110488, nsv3112960, nsv3110784
Samplessample285, sample273, sample275
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1282n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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