A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115969



Internal ID21299235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111918907..111924520hg38UCSC Ensembl
Innerchr7:111558962..111564575hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg385614
hg195614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083226
Samplessample65
Known GenesDOCK4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115969
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