A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114656



Internal ID21297922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168112271..168119948hg38UCSC Ensembl
Innerchr3:167830059..167837736hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg387678
hg197678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv823n145
Supporting Variantsnssv14107004
Samplessample246
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114656
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