A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114873



Internal ID21298139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:25903416..25908159hg38UCSC Ensembl
InnerchrX:25921533..25926276hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg384744
hg194744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1260n145
Supporting Variantsnssv14101684
Samplessample300
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114873
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