A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv366n106



Internal ID20159723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12413510..12413614hg38UCSC Ensembl
chr10:12455509..12455613hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120212, nsv1116632
SamplesKWS1, KWS2
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv366n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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