A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892932



Internal ID19183752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86611267..86620868hg38UCSC Ensembl
Outerchr16:86611267..86620868hg38UCSC Ensembl
Innerchr16:86644873..86654474hg19UCSC Ensembl
Outerchr16:86644873..86654474hg19UCSC Ensembl
Innerchr16:85202374..85211975hg18UCSC Ensembl
Outerchr16:85202374..85211975hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg389602
hg199602
hg189602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781642
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892932
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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