A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894000



Internal ID19184854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106657527..106667100hg38UCSC Ensembl
Outerchr4:106657527..106667100hg38UCSC Ensembl
Innerchr4:107578684..107588257hg19UCSC Ensembl
Outerchr4:107578684..107588257hg19UCSC Ensembl
Innerchr4:107798133..107807706hg18UCSC Ensembl
Outerchr4:107798133..107807706hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg389574
hg199574
hg189574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785719
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894000
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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