A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091500



Internal ID21289787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:19755481..19784442hg38UCSC Ensembl
Innerchr12:19908415..19937376hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3828962
hg1928962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110318
Supporting Variants
Samplessample51
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091500
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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