A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv803n100



Internal ID22786890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46489856hg38UCSC Ensembl
chr10:47047587..47153919hg19UCSC Ensembl
chr10:46467593..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3894014
hg19106333
hg18106333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051331, nsv1043350, nsv1036156, nsv1050078
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv803n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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