A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892916



Internal ID18837050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82707651..82732002hg38UCSC Ensembl
Outerchr16:82684425..82743191hg38UCSC Ensembl
Innerchr16:82741256..82765607hg19UCSC Ensembl
Outerchr16:82718030..82776796hg19UCSC Ensembl
Innerchr16:81298757..81323108hg18UCSC Ensembl
Outerchr16:81275531..81334297hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3858767
hg1958767
hg1858767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797332, essv25798910, essv25778548
Samples
Known GenesCDH13, MIR8058
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892916
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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