A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115564



Internal ID21298830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151410985..151419218hg38UCSC Ensembl
Innerchr5:150790546..150798779hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg388234
hg198234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109436, nssv14096809
Samplessample345, sample45
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115564
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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