A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892822



Internal ID19183642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28604387..28620264hg38UCSC Ensembl
Outerchr16:28604387..28620264hg38UCSC Ensembl
Innerchr16:28615708..28631585hg19UCSC Ensembl
Outerchr16:28615708..28631585hg19UCSC Ensembl
Innerchr16:28523209..28539086hg18UCSC Ensembl
Outerchr16:28523209..28539086hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3815878
hg1915878
hg1815878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798160, essv25798738
Samples
Known GenesSULT1A1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892822
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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