A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834185



Internal ID6159909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36626850..36788095hg19UCSC Ensembl
Outerchr22:34956796..35118041hg18UCSC Ensembl
Outerchr22:34951350..35112595hg17UCSC 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 StatusS
Merged Variants
Supporting Variantsnssv1456079
Samples
Known GenesAPOL1, APOL2, MYH9
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv834185
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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