A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1262n145



Internal ID22814278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30299446..30304662hg38UCSC Ensembl
chrX:30317563..30322779hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg385217
hg195217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116019, nsv3117134
Samplessample214, sample200, sample300, sample117
Known GenesNR0B1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1262n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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