A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113997



Internal ID21297263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24847030..24849585hg38UCSC Ensembl
Innerchr15:25092177..25094732hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382556
hg192556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv388n145
Supporting Variantsnssv14096053, nssv14096045, nssv14096067, nssv14096016
Samplessample93, sample78, sample82, sample59
Known GenesSNRPN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113997
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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