A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3012928



Internal ID15568632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94321565..94321565hg38UCSC Ensembl
chr14:94787902..94787902hg19UCSC Ensembl
chr14:93857655..93857655hg18UCSC Ensembl
chr14:93857655..93857655hg17UCSC Ensembl
Cytoband14q32.13
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 Variantsnsv479133
Supporting Variants
Samples
Known GenesSERPINA6
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)nssv3012928
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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