A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152458



Internal ID18856390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125426552..125426667hg38UCSC Ensembl
Outerchr11:125296448..125296563hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997064
SamplesKWB1
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152458
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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