A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113613



Internal ID21296879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:79587910..79598328hg38UCSC Ensembl
InnerchrX:78843407..78853825hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3810419
hg1910419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105051
Samplessample205
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113613
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer