A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4362n100



Internal ID22790449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10534998..10589451hg38UCSC Ensembl
chr21:10923006..10977459hg19UCSC Ensembl
chr21:9944877..9999330hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3854454
hg1954454
hg1854454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059519, nsv1062265, nsv1059820
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)dgv4362n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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