A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009039



Internal ID22070670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31108764..31225980hg38UCSC Ensembl
Outerchr12:31104761..31226462hg38UCSC Ensembl
Innerchr12:31261698..31378914hg19UCSC Ensembl
Outerchr12:31257695..31379396hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38121702
hg19121702
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154822
Supporting Variants
Samples
Known GenesDDX11
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009039
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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