A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082988



Internal ID21282717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15469209..15473955hg38UCSC Ensembl
Innerchr6:15469440..15474186hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384747
hg194747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115326
Supporting Variants
Samplessample331
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082988
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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