A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112960



Internal ID21296226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139929033..139934291hg38UCSC Ensembl
InnerchrX:139011192..139016450hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1282n145
Supporting Variantsnssv14101668
Samplessample285
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112960
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