A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778809



Internal ID18827992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4204149..4234996hg38UCSC Ensembl
Innerchr3:4245833..4276680hg19UCSC Ensembl
Innerchr3:4220833..4251680hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3830848
hg1930848
hg1830848
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893630
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778809
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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