A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1276n145



Internal ID22814292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131165097..131169253hg38UCSC Ensembl
chrX:130299071..130303227hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115491, nsv3115537
Samplessample267, sample23
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1276n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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