A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv891n100



Internal ID22786978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65563025..65584185hg38UCSC Ensembl
chr10:67322783..67343943hg19UCSC Ensembl
chr10:66992789..67013949hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3821161
hg1921161
hg1821161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051687, nsv1047766
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)dgv891n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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