A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083056



Internal ID21283686
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 StatusS
Merged Variantsnsv3113144
Supporting Variants
Samplessample349
Known GenesPLEKHG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083056
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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