A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv721n106



Internal ID20160078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110209275..110214775hg38UCSC Ensembl
chr11:110080000..110085500hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1132352, nsv1124647
SamplesKWS1, KWS2
Known GenesRDX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv721n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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