A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800667



Internal ID19162771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17338052..17351832hg38UCSC Ensembl
Innerchr21:18710371..18724151hg19UCSC Ensembl
Innerchr21:17632242..17646022hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3813781
hg1913781
hg1813781
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893379
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800667
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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