A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894116



Internal ID19184970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3848742..3868844hg38UCSC Ensembl
Outerchr5:3848742..3868844hg38UCSC Ensembl
Innerchr5:3848856..3868958hg19UCSC Ensembl
Outerchr5:3848856..3868958hg19UCSC Ensembl
Innerchr5:3901856..3921958hg18UCSC Ensembl
Outerchr5:3901856..3921958hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3820103
hg1920103
hg1820103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780266
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894116
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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