A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1266n145



Internal ID22814282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54529031..54532535hg38UCSC Ensembl
chrX:54555464..54558968hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg383505
hg193505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116625, nsv3110656, nsv3116751
Samplessample184, sample312, sample81, sample147, sample275
Known GenesGNL3L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1266n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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