A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv666n106



Internal ID22794494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65216029..65216929hg38UCSC Ensembl
chr11:64983500..64984400hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1143543, nsv1136133
SamplesKWS2, KWS1
Known GenesSLC22A20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv666n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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