A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv811n100



Internal ID20152427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46446149..46489856hg38UCSC Ensembl
chr10:47058780..47103613hg19UCSC Ensembl
chr10:46478786..46523619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3843708
hg1944834
hg1844834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043941, nsv1044728, nsv1050503
Samples
Known GenesLINC00842, 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)dgv811n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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