A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111050



Internal ID18935686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:26680299..26680389hg38UCSC Ensembl
Outerchr11:26701846..26701936hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962249
SamplesKWS1
Known GenesSLC5A12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111050
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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