A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894115



Internal ID19184969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3004470..3025338hg38UCSC Ensembl
Outerchr5:2999404..3025338hg38UCSC Ensembl
Innerchr5:3004584..3025452hg19UCSC Ensembl
Outerchr5:2999518..3025452hg19UCSC Ensembl
Innerchr5:3057584..3078452hg18UCSC Ensembl
Outerchr5:3052518..3078452hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3825935
hg1925935
hg1825935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783382, essv25783548, essv25780227, essv25787685, essv25797010, essv25782179, essv25800477, essv25782674
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894115
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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