A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv470669



Internal ID6060120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101243384..101303361hg19UCSC Ensembl
Innerchr14:100313137..100373114hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv547611
SamplesHGDP00978
Known GenesMEG3, MIR2392
Method
AnalysisOverlapping CNVs were merged. The positions are based on the farthest SNPs observed anomg any individuals with the CNV.
PlatformIllumina HumanHap550 Genotyping BeadChip v1 + v3
Comments
ReferenceJakobsson et al 2008
Pubmed ID18288195
Accession Number(s)nsv470669
Frequency
Sample Size443
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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