A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089190



Internal ID21279087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71602162..71604599hg38UCSC Ensembl
Innerchr6:72311865..72314302hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112179
Supporting Variants
Samplessample278
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089190
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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