A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1667



Internal ID15546230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91955555..91989603hg38UCSC Ensembl
Outerchr15:92498785..92532833hg19UCSC Ensembl
Outerchr15:90299789..90333837hg18UCSC Ensembl
Outerchr15:90299789..90333837hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385698
hg195698
hg185698
hg175698
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4174
SamplesNA12878
Known GenesSLCO3A1
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)nsv1667
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