A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832876



Internal ID6158600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101141170..101319256hg19UCSC Ensembl
Outerchr14:100210923..100389009hg18UCSC Ensembl
Outerchr14:100210923..100389009hg17UCSC Ensembl
Cytoband14q32.2
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 Variantsnssv1451154, nssv1451155
Samples
Known GenesDLK1, MEG3, MIR2392, MIR770
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832876
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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