A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv649n100



Internal ID20152265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26861..228735hg38UCSC Ensembl
chr10:72797..274675hg19UCSC Ensembl
chr10:62797..264675hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38201875
hg19201879
hg18201879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044775, nsv1048232, nsv1040332, nsv1047868
Samples
Known GenesTUBB8, ZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv649n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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