A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086449



Internal ID21270112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15466330..15473873hg38UCSC Ensembl
Innerchr6:15466561..15474104hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387544
hg197544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113503
Supporting Variants
Samplessample147
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086449
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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