A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894159



Internal ID19185228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28621186..28659108hg38UCSC Ensembl
Outerchr5:28621186..28662221hg38UCSC Ensembl
Innerchr5:28621293..28659215hg19UCSC Ensembl
Outerchr5:28621293..28662328hg19UCSC Ensembl
Innerchr5:28657050..28694972hg18UCSC Ensembl
Outerchr5:28657050..28698085hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3841036
hg1941036
hg1841036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796685, essv25781609
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894159
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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