A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv646n100



Internal ID22786733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26861..115453hg38UCSC Ensembl
chr10:72797..161393hg19UCSC Ensembl
chr10:62797..151393hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3888593
hg1988597
hg1888597
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041943, nsv1053736
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)dgv646n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer