A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893882



Internal ID19184702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11569540..11713299hg38UCSC Ensembl
Outerchr4:11569540..11713299hg38UCSC Ensembl
Innerchr4:11571164..11714923hg19UCSC Ensembl
Outerchr4:11571164..11714923hg19UCSC Ensembl
Innerchr4:11180262..11324021hg18UCSC Ensembl
Outerchr4:11180262..11324021hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38143760
hg19143760
hg18143760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799027
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893882
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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