A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134151



Internal ID19263050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68456762..68456841hg38UCSC Ensembl
Outerchr11:68224230..68224309hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970494
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134151
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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