A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4356n100



Internal ID20155972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10448879..10643715hg38UCSC Ensembl
chr21:10868742..11063578hg19UCSC Ensembl
chr21:9890613..10085449hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38194837
hg19194837
hg18194837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064468, nsv1057371, nsv1065873
Samples
Known GenesBAGE, BAGE2, 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)dgv4356n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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