A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv479007



Internal ID15578433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74070799..74070799hg38UCSC Ensembl
chr2:74297926..74297926hg19UCSC Ensembl
chr2:74151434..74151434hg18UCSC Ensembl
chr2:74209581..74209581hg17UCSC Ensembl
Cytoband2p13.1
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 Variantsnssv3013559
Samples
Known GenesTET3
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)nsv479007
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