A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4373n100



Internal ID20155989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10338676..10473197hg38UCSC Ensembl
chr21:11039260..11173781hg19UCSC Ensembl
chr21:10061131..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38134522
hg19134522
hg18134522
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065941, nsv1057249, nsv1056567
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4373n100
Frequency
Sample Size29084
Observed Gain35
Observed Loss10
Observed Complex0
Frequencyn/a


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