A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n67



Internal ID6316439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103529485..103577142hg19UCSC Ensembl
chr10:103519475..103567132hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv825547, nsv825546
SamplesNA18969, NA18973
Known GenesFGF8, MGEA5, NPM3
Method
Analysis
Platform
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)dgv171n67
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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