A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5346



Internal ID15543210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4854208..4887814hg38UCSC Ensembl
Outerchr11:4875438..4909044hg19UCSC Ensembl
Outerchr11:4832014..4865620hg18UCSC Ensembl
Outerchr11:4832014..4865620hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385682
hg195682
hg185682
hg175682
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7651
Supporting Variants
SamplesNA19129
Known GenesOR51T1
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)nssv5346
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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