A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4357n100



Internal ID22790444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10548222..10611996hg38UCSC Ensembl
chr21:10900461..10964235hg19UCSC Ensembl
chr21:9922332..9986106hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3863775
hg1963775
hg1863775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059286, nsv1065629
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)dgv4357n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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