A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832526



Internal ID6158250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:117530234..117723821hg19UCSC Ensembl
Outerchr12:116014617..116208204hg18UCSC Ensembl
Outerchr12:115992954..116186541hg17UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1450032, nssv1450031, nssv1450030
Samples
Known GenesFBXO21, NOS1, TESC
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832526
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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