A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2413n106



Internal ID22796241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45796986..45799186hg38UCSC Ensembl
chr21:47216900..47219100hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118680, nsv1115620
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2413n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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