A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893881



Internal ID19184701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11438322..11458256hg38UCSC Ensembl
Outerchr4:11438322..11459215hg38UCSC Ensembl
Innerchr4:11439946..11459880hg19UCSC Ensembl
Outerchr4:11439946..11460839hg19UCSC Ensembl
Innerchr4:11049044..11068978hg18UCSC Ensembl
Outerchr4:11049044..11069937hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3820894
hg1920894
hg1820894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796025, essv25784204
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893881
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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