A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115397



Internal ID21298663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52672151..52673577hg38UCSC Ensembl
Innerchr5:51967985..51969411hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381427
hg191427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096798
Samplessample44
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115397
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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