A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112710



Internal ID21295976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169064281..169065866hg38UCSC Ensembl
Innerchr6:169464376..169465961hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381586
hg191586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1086n145
Supporting Variantsnssv14083675
Samplessample56
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112710
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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