A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118136



Internal ID21301402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:162150171..162155109hg38UCSC Ensembl
Innerchr2:163006681..163011619hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg384939
hg194939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104660
Samplessample145
Known GenesGCG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118136
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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