A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4363n100



Internal ID20155979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10420787..10576547hg38UCSC Ensembl
chr21:10935910..11091670hg19UCSC Ensembl
chr21:9957781..10113541hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38155761
hg19155761
hg18155761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065276, nsv1057984
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)dgv4363n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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