A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4353n100



Internal ID22790440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10458894..10775598hg38UCSC Ensembl
chr21:10736859..11053563hg19UCSC Ensembl
chr21:9758730..10075434hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38316705
hg19316705
hg18316705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060258, nsv1056764, nsv1057950, nsv1057883, nsv1066007, nsv1064110, nsv1062344, nsv1063501
Samples
Known GenesBAGE2, 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)dgv4353n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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