A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1487



Internal ID15199364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:35228589..35258344hg38UCSC Ensembl
Outerchr15:35520790..35550545hg19UCSC Ensembl
Outerchr15:33308082..33337837hg18UCSC Ensembl
Outerchr15:33308082..33337837hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389511
hg199511
hg189511
hg179511
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5549
SamplesNA19129
Known GenesANP32AP1
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)nsv1487
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