A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830551



Internal ID6156275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:170746922..170922033hg19UCSC Ensembl
Outerchr5:170679527..170854638hg18UCSC Ensembl
Outerchr5:170679527..170854638hg17UCSC Ensembl
Cytoband5q35.1
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 Variantsnssv1445149, nssv1445148
Samples
Known GenesFGF18, MIR3912, NPM1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv830551
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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