A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118090



Internal ID21301356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7146558..7715750hg38UCSC Ensembl
Innerchr20:7127205..7696397hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38569193
hg19569193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100804
Samplessample397
Known GenesMIR8062
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118090
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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