A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086948



Internal ID21291706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102920371..102932909hg38UCSC Ensembl
Innerchr8:103932599..103945137hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3812539
hg1912539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117317
Supporting Variants
Samplessample78
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086948
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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