A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083486



Internal ID21269485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117906260..117909780hg38UCSC Ensembl
Innerchr6:118227423..118230943hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg383521
hg193521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113156
Supporting Variants
Samplessample14
Known GenesSLC35F1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083486
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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