A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111207



Internal ID21294473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132148743..132151056hg38UCSC Ensembl
Innerchr7:131833502..131835815hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382314
hg192314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084296
Samplessample146
Known GenesPLXNA4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111207
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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