A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892866



Internal ID19183686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58864281..58880160hg38UCSC Ensembl
Outerchr16:58861935..58884534hg38UCSC Ensembl
Innerchr16:58898185..58914064hg19UCSC Ensembl
Outerchr16:58895839..58918438hg19UCSC Ensembl
Innerchr16:57455686..57471565hg18UCSC Ensembl
Outerchr16:57453340..57475939hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3822600
hg1922600
hg1822600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798957, essv25782307, essv25799877, essv25782103, essv25798743, essv25799520, essv25784417
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892866
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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