A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113342



Internal ID21296608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132773935..132776977hg38UCSC Ensembl
Innerchr8:133786181..133789223hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg383043
hg193043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087196
Samplessample138
Known GenesPHF20L1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113342
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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