A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv478998



Internal ID15231738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70410626..70410626hg38UCSC Ensembl
chr11:70256732..70256732hg19UCSC Ensembl
chr11:69934380..69934380hg18UCSC Ensembl
chr11:69934380..69934380hg17UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3018277
Samples
Known GenesCTTN
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA singleton. The coordinate provided is from the mappable member of a fosmid end sequence pair, and indicates the genomic vicinity of a novel sequence insertion
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv478998
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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