A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091606



Internal ID21292022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:70070550..70151885hg38UCSC Ensembl
Innerchr12:70464330..70545665hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3881336
hg1981336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111757
Supporting Variants
Samplessample82
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091606
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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