A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv479176



Internal ID15231916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206260315..206260315hg38UCSC Ensembl
chr2:207125039..207125039hg19UCSC Ensembl
chr2:206833284..206833284hg18UCSC Ensembl
chr2:206950545..206950545hg17UCSC Ensembl
Cytoband2q33.3
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 Variantsnssv3016014
Samples
Known GenesGPR1-AS
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)nsv479176
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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