A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801311



Internal ID19180101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4084575..4098215hg38UCSC Ensembl
Innerchr3:4126259..4139899hg19UCSC Ensembl
Innerchr3:4101259..4114899hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3813641
hg1913641
hg1813641
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893638
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801311
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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