A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv405



Internal ID15548720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:80380871..80425639hg38UCSC Ensembl
Outerchr11:80091915..80136683hg19UCSC Ensembl
Outerchr11:79769563..79814331hg18UCSC Ensembl
Outerchr11:79769563..79814331hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3844769
hg1944769
hg1844769
hg1744769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8939
SamplesNA12156
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)nsv405
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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