A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832114



Internal ID6157838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:34424428..34607851hg19UCSC Ensembl
Outerchr11:34381004..34564427hg18UCSC Ensembl
Outerchr11:34381004..34564427hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1449107
Samples
Known GenesCAT, ELF5
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832114
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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