A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116858



Internal ID21300124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52178101..52181716hg38UCSC Ensembl
Innerchr15:52470298..52473913hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097177
Samplessample349
Known GenesGNB5, LOC100129973
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116858
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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