A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2858



Internal ID15541703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11242748..11248493hg38UCSC Ensembl
Outerchr11:11264295..11270040hg19UCSC Ensembl
Outerchr11:11220871..11226616hg18UCSC Ensembl
Outerchr11:11220871..11226616hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385884
hg195884
hg185884
hg175884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7677
Supporting Variants
SamplesNA18555
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)nssv2858
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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