A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7651



Internal ID15552682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4825578..4887814hg38UCSC Ensembl
Outerchr11:4846808..4909044hg19UCSC Ensembl
Outerchr11:4803384..4865620hg18UCSC Ensembl
Outerchr11:4803384..4865620hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386802
hg196802
hg186802
hg176802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1925, nssv5346
SamplesNA18555, NA19129
Known GenesOR51S1, OR51T1
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)nsv7651
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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