A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv403



Internal ID15548698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:79917704..79951476hg38UCSC Ensembl
Outerchr11:79628747..79662519hg19UCSC Ensembl
Outerchr11:79306395..79340167hg18UCSC Ensembl
Outerchr11:79306395..79340167hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385663
hg195663
hg185663
hg175663
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8938
SamplesNA12156
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)nsv403
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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