A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1259n145



Internal ID22814275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19072521..19075135hg38UCSC Ensembl
chrX:19090639..19093253hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg382615
hg192615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114171, nsv3117367, nsv3114706
Samplessample380, sample91, sample140, sample81, sample300, sample299
Known GenesGPR64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1259n145
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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