A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111901



Internal ID21295167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61525615..61542466hg38UCSC Ensembl
Innerchr6:62235520..62252371hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3816852
hg1916852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1041n145
Supporting Variantsnssv14083090
Samplessample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111901
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