A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3015768



Internal ID15566793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50269204..50269204hg38UCSC Ensembl
chr22:50707633..50707633hg19UCSC Ensembl
chr22:49049760..49049760hg18UCSC Ensembl
chr22:49010090..49010090hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv475003
Supporting Variants
SamplesNA18956
Known GenesMAPK11
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)nssv3015768
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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