A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1258n145



Internal ID22814274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11428850..11430494hg38UCSC Ensembl
chrX:11446970..11448614hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112063, nsv3110370
Samplessample287, sample34
Known GenesARHGAP6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1258n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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