A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892868



Internal ID19183688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59906284..59930028hg38UCSC Ensembl
Outerchr16:59906284..59930028hg38UCSC Ensembl
Innerchr16:59940188..59963932hg19UCSC Ensembl
Outerchr16:59940188..59963932hg19UCSC Ensembl
Innerchr16:58497689..58521433hg18UCSC Ensembl
Outerchr16:58497689..58521433hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3823745
hg1923745
hg1823745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798089
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892868
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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