A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111808



Internal ID21295074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26970856..27028322hg38UCSC Ensembl
Innerchr6:26938635..26996101hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3857467
hg1957467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087654
Samplessample206
Known GenesLINC00240, LOC100270746
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111808
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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