A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832879



Internal ID6158603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102482074..102549316hg19UCSC Ensembl
Outerchr14:101551827..101619069hg18UCSC Ensembl
Outerchr14:101551827..101619069hg17UCSC Ensembl
Cytoband14q32.31
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 Variantsnssv1451158
Samples
Known GenesDYNC1H1, HSP90AA1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832879
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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