A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784618



Internal ID19166973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4093768..4198269hg38UCSC Ensembl
Innerchr3:4135452..4239953hg19UCSC Ensembl
Innerchr3:4110452..4214953hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38104502
hg19104502
hg18104502
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893628
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784618
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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