A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4370n100



Internal ID20155986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10386269..10529640hg38UCSC Ensembl
chr21:10982817..11126188hg19UCSC Ensembl
chr21:10004688..10148059hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38143372
hg19143372
hg18143372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058893, nsv1066344, nsv1055301, nsv1059585
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4370n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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