A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv726n100



Internal ID20152342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43079488..43095609hg38UCSC Ensembl
chr10:43574936..43591057hg19UCSC Ensembl
chr10:42894942..42911063hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3816122
hg1916122
hg1816122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049670, nsv1050563
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv726n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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