A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111143



Internal ID21294409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85513525..85516266hg38UCSC Ensembl
Innerchr15:86056756..86059497hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382742
hg192742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097100
Samplessample296
Known GenesAKAP13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111143
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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