A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv732n106



Internal ID20160089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118910892..118910946hg38UCSC Ensembl
chr11:118781601..118781655hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1113442, nsv1145571
SamplesKWS2, KWS1
Known GenesBCL9L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv732n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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