A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089221



Internal ID21279658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145383027..145384907hg38UCSC Ensembl
Innerchr6:145704163..145706043hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111150
Supporting Variants
Samplessample287
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089221
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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