A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1489



Internal ID15546052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:35360604..35395540hg38UCSC Ensembl
Outerchr15:35652805..35687741hg19UCSC Ensembl
Outerchr15:33440097..33475033hg18UCSC Ensembl
Outerchr15:33440097..33475033hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg386056
hg196056
hg186056
hg176056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1247
SamplesNA19240
Known GenesDPH6, MIR3942
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)nsv1489
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