A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5376



Internal ID15543038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110918245..110948417hg38UCSC Ensembl
Outerchr11:110788969..110819141hg19UCSC Ensembl
Outerchr11:110294179..110324351hg18UCSC Ensembl
Outerchr11:110294179..110324351hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg389099
hg199099
hg189099
hg179099
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv487
Supporting Variants
SamplesNA19129
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)nssv5376
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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