A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893374



Internal ID18837508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:16442717..16561877hg38UCSC Ensembl
Outerchr21:16442717..16561877hg38UCSC Ensembl
Innerchr21:17815037..17934197hg19UCSC Ensembl
Outerchr21:17815037..17934197hg19UCSC Ensembl
Innerchr21:16736908..16856068hg18UCSC Ensembl
Outerchr21:16736908..16856068hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38119161
hg19119161
hg18119161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799386
Samples
Known GenesLINC00478, MIR99A, MIRLET7C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893374
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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