A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1585



Internal ID15199462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:69443667..69470113hg38UCSC Ensembl
Outerchr15:69736006..69762452hg19UCSC Ensembl
Outerchr15:67523060..67549506hg18UCSC Ensembl
Outerchr15:67523060..67549506hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3813415
hg1913415
hg1813415
hg1713415
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10933
SamplesNA15510
Known GenesKIF23, RPLP1
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)nsv1585
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