A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834186



Internal ID6159910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36731923..36906812hg19UCSC Ensembl
Outerchr22:35061869..35236758hg18UCSC Ensembl
Outerchr22:35056423..35231312hg17UCSC Ensembl
Cytoband22q12.3
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 Variantsnssv1456084, nssv1456080, nssv1456082, nssv1456083, nssv1456081
Samples
Known GenesFOXRED2, MYH9, TXN2
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv834186
Frequency
Sample Size95
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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