A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv477728



Internal ID15577154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33695117..33695117hg38UCSC Ensembl
chr19:34186022..34186022hg19UCSC Ensembl
chr19:38877862..38877862hg18UCSC Ensembl
chr19:38877862..38877862hg17UCSC Ensembl
Cytoband19q13.11
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 Variantsnssv3015327
SamplesNA18517
Known GenesCHST8
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)nsv477728
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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