A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087717



Internal ID21275357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78811188..78814066hg38UCSC Ensembl
Innerchr6:79520905..79523783hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382879
hg192879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114871
Supporting Variants
Samplessample221
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087717
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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