A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893388



Internal ID19184208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21764717..21916685hg38UCSC Ensembl
Outerchr21:21764717..21916685hg38UCSC Ensembl
Innerchr21:23137037..23289005hg19UCSC Ensembl
Outerchr21:23137037..23289005hg19UCSC Ensembl
Innerchr21:22058908..22210876hg18UCSC Ensembl
Outerchr21:22058908..22210876hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38151969
hg19151969
hg18151969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798247
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893388
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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