A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893371



Internal ID18837505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14104569..14339246hg38UCSC Ensembl
Outerchr21:14104569..14339246hg38UCSC Ensembl
Innerchr21:15476890..15711567hg19UCSC Ensembl
Outerchr21:15476890..15711567hg19UCSC Ensembl
Innerchr21:14398761..14633438hg18UCSC Ensembl
Outerchr21:14398761..14633438hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38234678
hg19234678
hg18234678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788387
Samples
Known GenesABCC13, LIPI, RBM11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893371
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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