A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133165



Internal ID19270019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:58371748..58404373hg38UCSC Ensembl
Outerchr11:58139221..58171846hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3832626
hg1932626
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988014
SamplesKWS1
Known GenesOR5B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133165
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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