A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790359



Internal ID19167075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89855732..90289369hg38UCSC Ensembl
Innerchr3:89904882..90338519hg19UCSC Ensembl
Innerchr3:89987572..90421209hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38433638
hg19433638
hg18433638
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893741
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790359
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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