A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952759



Internal ID16954946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:128696006..128745405hg38UCSC Ensembl
Outerchr11:128565901..128615300hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3849400
hg1949400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999642
SamplesBILGI_BIOE
Known GenesFLI1, SENCR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952759
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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