A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667



Internal ID15203813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:24804253..24833243hg38UCSC Ensembl
Outerchr7:24843872..24872862hg19UCSC Ensembl
Outerchr7:24810397..24839387hg18UCSC Ensembl
Outerchr7:24617112..24646102hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3810733
hg1910733
hg1810733
hg1710733
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510
SamplesNA12878
Known GenesOSBPL3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv5667
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