A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115259



Internal ID21298525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56906772..56909706hg38UCSC Ensembl
Innerchr4:57772938..57775872hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382935
hg192935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089306
Samplessample111
Known GenesREST
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115259
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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