A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110787



Internal ID21294053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68701312..68726776hg38UCSC Ensembl
Innerchr7:68166299..68191763hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3825465
hg1925465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085491
Samplessample270
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110787
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