A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv805n100



Internal ID22786892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46467768..46489856hg38UCSC Ensembl
chr10:47055642..47081683hg19UCSC Ensembl
chr10:46475648..46501689hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3822089
hg1926042
hg1826042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043478, nsv1046849, nsv1049223, nsv1051775, nsv1039724
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv805n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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