A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1288n145



Internal ID22814304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154748793..154753416hg38UCSC Ensembl
chrX:153977068..153981691hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384624
hg194624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112520, nsv3118010
Samplessample359, sample137
Known GenesGAB3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1288n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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