A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv647n100



Internal ID22786734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26861..118720hg38UCSC Ensembl
chr10:72797..164660hg19UCSC Ensembl
chr10:62797..154660hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3891860
hg1991864
hg1891864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048591, nsv1050135, nsv1042793, nsv1053793, nsv1046504, nsv1038030, nsv1051040, nsv1054622, nsv1045283
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv647n100
Frequency
Sample Size11257
Observed Gain37
Observed Loss0
Observed Complex0
Frequencyn/a


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