A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008267



Internal ID6720377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10475568..10476520hg38UCSC Ensembl
Outerchr21:11035937..11036889hg19UCSC Ensembl
Outerchr21:10057808..10058760hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38953
hg19953
hg18953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564927
SamplesHuRef
Known GenesBAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008267
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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