A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832095



Internal ID6157819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:27538626..27715739hg19UCSC Ensembl
Outerchr11:27495202..27672315hg18UCSC Ensembl
Outerchr11:27495202..27672315hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1449065, nssv1449064
Samples
Known GenesBDNF, BDNF-AS1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832095
Frequency
Sample Size95
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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