A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089191



Internal ID21279086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148073867..148076315hg38UCSC Ensembl
Innerchr6:148395003..148397451hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382449
hg192449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113802
Supporting Variants
Samplessample278
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089191
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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