A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv791n100



Internal ID22786878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47020164..47108045hg19UCSC Ensembl
chr10:46440170..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1987882
hg1887882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044357, nsv1050418, nsv1043767, nsv1036939
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)dgv791n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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