A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv450



Internal ID15549215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:95678966..95711605hg38UCSC Ensembl
Outerchr11:95412130..95444769hg19UCSC Ensembl
Outerchr11:95051778..95084417hg18UCSC Ensembl
Outerchr11:95051778..95084417hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388364
hg198364
hg188364
hg178364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1032
SamplesNA19240
Known Genes
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)nsv450
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