A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893880



Internal ID19184700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10870031..11214614hg38UCSC Ensembl
Outerchr4:10870031..11214614hg38UCSC Ensembl
Innerchr4:10871655..11216238hg19UCSC Ensembl
Outerchr4:10871655..11216238hg19UCSC Ensembl
Innerchr4:10480753..10825336hg18UCSC Ensembl
Outerchr4:10480753..10825336hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38344584
hg19344584
hg18344584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791394
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893880
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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