A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833499



Internal ID6159223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57070693..57288410hg19UCSC Ensembl
Outerchr17:54425475..54643192hg18UCSC Ensembl
Outerchr17:54425475..54643192hg17UCSC Ensembl
Cytoband17q22
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 Variantsnssv1453600
Samples
Known GenesMIR301A, MIR454, PRR11, SKA2, SMG8, TRIM37
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833499
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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