A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111659



Internal ID21294925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11806955..11855024hg38UCSC Ensembl
Innerchr10:11848954..11897023hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3848070
hg1948070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n145
Supporting Variantsnssv14090162
Samplessample145
Known GenesPROSER2, PROSER2-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111659
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