A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893874



Internal ID19184694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10048076..10061225hg38UCSC Ensembl
Outerchr4:10048076..10061225hg38UCSC Ensembl
Innerchr4:10049700..10062849hg19UCSC Ensembl
Outerchr4:10049700..10062849hg19UCSC Ensembl
Innerchr4:9658798..9671947hg18UCSC Ensembl
Outerchr4:9658798..9671947hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3813150
hg1913150
hg1813150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786639
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893874
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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