A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv490



Internal ID15202969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:111315172..111359869hg38UCSC Ensembl
Outerchr11:111185897..111230594hg19UCSC Ensembl
Outerchr11:110691107..110735804hg18UCSC Ensembl
Outerchr11:110691107..110735804hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3844698
hg1944698
hg1844698
hg1744698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8963
SamplesNA12156
Known GenesMIR4491, POU2AF1
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)nsv490
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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