A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784714



Internal ID19173809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17098391..17319089hg38UCSC Ensembl
Innerchr21:18470709..18691408hg19UCSC Ensembl
Innerchr21:17392580..17613279hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38220699
hg19220700
hg18220700
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893376
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784714
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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