A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114670



Internal ID21297936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43652728..43656655hg38UCSC Ensembl
InnerchrX:43511976..43515903hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg383928
hg193928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1264n145
Supporting Variantsnssv14101827
Samplessample400
Known GenesMAOA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114670
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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