A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4361n100



Internal ID22790448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10502083..10591182hg38UCSC Ensembl
chr21:10921275..11010374hg19UCSC Ensembl
chr21:9943146..10032245hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3889100
hg1989100
hg1889100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063986, nsv1057872, nsv1056354, nsv1061947, nsv1058791
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)dgv4361n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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