A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092929



Internal ID21271358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73090396..73147095hg38UCSC Ensembl
Innerchr12:73484176..73540875hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3856700
hg1956700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111957
Supporting Variants
Samplessample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092929
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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