A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833637



Internal ID6159361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:42430299..42584879hg19UCSC Ensembl
Outerchr18:40684297..40838877hg18UCSC Ensembl
Outerchr18:40684297..40838877hg17UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1453991
Samples
Known GenesMIR4319, SETBP1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833637
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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