A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778742



Internal ID18833587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89483618..89497459hg38UCSC Ensembl
Innerchr3:89532768..89546609hg19UCSC Ensembl
Innerchr3:89615458..89629299hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3813842
hg1913842
hg1813842
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893739
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778742
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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