A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010297



Internal ID22071928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110796150..110797921hg38UCSC Ensembl
Outerchr12:110788037..110800645hg38UCSC Ensembl
Innerchr12:111233954..111235725hg19UCSC Ensembl
Outerchr12:111225842..111238449hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3812609
hg1912608
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154855
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010297
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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