A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112850



Internal ID21296116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47657106..47663577hg38UCSC Ensembl
Innerchr7:47696704..47703175hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg386472
hg196472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084218
Samplessample134
Known GenesC7orf65
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112850
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