A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147628



Internal ID19202782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:6187069..6190970hg38UCSC Ensembl
Outerchr11:6208299..6212200hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996418
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147628
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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