A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113144



Internal ID21296410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150598670..150601139hg38UCSC Ensembl
Innerchr6:150919806..150922275hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382470
hg192470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083056
Samplessample349
Known GenesPLEKHG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113144
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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