A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951066



Internal ID16953253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:108154174..108159373hg38UCSC Ensembl
Outerchr11:108024901..108030100hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999613
SamplesBILGI_BIOE
Known GenesNPAT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951066
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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