A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113402



Internal ID21296668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39035184..39045398hg38UCSC Ensembl
Innerchr7:39074784..39084998hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3810215
hg1910215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084963
Samplessample394
Known GenesPOU6F2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113402
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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