A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892864



Internal ID19183684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57592999..57603556hg38UCSC Ensembl
Outerchr16:57592999..57603556hg38UCSC Ensembl
Innerchr16:57626911..57637468hg19UCSC Ensembl
Outerchr16:57626911..57637468hg19UCSC Ensembl
Innerchr16:56184412..56194969hg18UCSC Ensembl
Outerchr16:56184412..56194969hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3810558
hg1910558
hg1810558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798941, essv25799372
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892864
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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