A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800227



Internal ID19179559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39051545..39065027hg38UCSC Ensembl
Innerchr21:40423471..40436953hg19UCSC Ensembl
Innerchr21:39345341..39358823hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3813483
hg1913483
hg1813483
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893410
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800227
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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