A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114064



Internal ID21297330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106109961..106114077hg38UCSC Ensembl
Innerchr7:105750407..105754523hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1122n145
Supporting Variantsnssv14086778
Samplessample348
Known GenesSYPL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114064
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