A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833382



Internal ID6159106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:17124329..17305683hg19UCSC Ensembl
Outerchr17:17065054..17246408hg18UCSC Ensembl
Outerchr17:17065054..17246408hg17UCSC Ensembl
Cytoband17p11.2
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 Variantsnssv1453133, nssv1453132
Samples
Known GenesCOPS3, FLCN, NT5M
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833382
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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