A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091319



Internal ID21274882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:58589012..58591700hg38UCSC Ensembl
Innerchr12:58982794..58985482hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg382689
hg192689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111480
Supporting Variants
Samplessample213
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091319
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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