A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894126



Internal ID19185195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12227022..12389639hg38UCSC Ensembl
Outerchr5:12227022..12407240hg38UCSC Ensembl
Innerchr5:12227134..12389751hg19UCSC Ensembl
Outerchr5:12227134..12407352hg19UCSC Ensembl
Innerchr5:12280134..12442751hg18UCSC Ensembl
Outerchr5:12280134..12460352hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38180219
hg19180219
hg18180219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797259, essv25782885
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894126
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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