A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893367



Internal ID19184187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13190193..13915563hg38UCSC Ensembl
Outerchr21:13190193..13915563hg38UCSC Ensembl
Innerchr21:14562514..15287884hg19UCSC Ensembl
Outerchr21:14562514..15287884hg19UCSC Ensembl
Innerchr21:13484385..14209755hg18UCSC Ensembl
Outerchr21:13484385..14209755hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38725371
hg19725371
hg18725371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788386
Samples
Known GenesC21orf15, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893367
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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