A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117162



Internal ID21300428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159725977..159729099hg38UCSC Ensembl
Innerchr6:160147009..160150131hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383123
hg193123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1081n145
Supporting Variantsnssv14083057
Samplessample349
Known GenesWTAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117162
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