A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116008



Internal ID21299274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117906388..117909066hg38UCSC Ensembl
Innerchr6:118227551..118230229hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg382679
hg192679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1064n145
Supporting Variantsnssv14087730
Samplessample224
Known GenesSLC35F1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116008
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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