A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4350n100



Internal ID22790437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10545409..10775598hg38UCSC Ensembl
chr21:10736859..10967048hg19UCSC Ensembl
chr21:9758730..9988919hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38230190
hg19230190
hg18230190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057621, nsv1065332, nsv1057962, nsv1058986, nsv1059412, nsv1057670, nsv1065006, nsv1059827
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4350n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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