A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894131



Internal ID19185200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12575070..13592862hg38UCSC Ensembl
Outerchr5:12575070..13592862hg38UCSC Ensembl
Innerchr5:12575182..13592971hg19UCSC Ensembl
Outerchr5:12575182..13592971hg19UCSC Ensembl
Innerchr5:12628182..13645971hg18UCSC Ensembl
Outerchr5:12628182..13645971hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381017793
hg191017790
hg181017790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788227
Samples
Known GenesCT49
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894131
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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