A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4394n100



Internal ID22790481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18998152..19032598hg38UCSC Ensembl
chr21:20370470..20404917hg19UCSC Ensembl
chr21:19292341..19326788hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3834447
hg1934448
hg1834448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063400, nsv1060659
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)dgv4394n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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