A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894036



Internal ID19184890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132912583..132997591hg38UCSC Ensembl
Outerchr4:132912583..132997591hg38UCSC Ensembl
Innerchr4:133833738..133918746hg19UCSC Ensembl
Outerchr4:133833738..133918746hg19UCSC Ensembl
Innerchr4:134053188..134138196hg18UCSC Ensembl
Outerchr4:134053188..134138196hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3885009
hg1985009
hg1885009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786301
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894036
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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