A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv588n106



Internal ID20159945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12130997..12131321hg38UCSC Ensembl
chr11:12152544..12152868hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111470, nsv1110494, nsv1135428
SamplesKWS2, KWS1
Known GenesMICAL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv588n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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