A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv724n106



Internal ID20160081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935087..113935461hg38UCSC Ensembl
chr11:113805809..113806183hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1134994, nsv1121110
SamplesKWS2
Known GenesHTR3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv724n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer