A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv473876



Internal ID15573309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89786412..89786412hg38UCSC Ensembl
chr9:92487859..92487859hg19UCSC Ensembl
chr9:91627679..91627679hg18UCSC Ensembl
chr9:89667413..89667413hg17UCSC Ensembl
Cytoband9q22.2
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 Variantsnssv3014304
SamplesNA12156
Known Genes
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)nsv473876
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer