A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892765



Internal ID18836899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5529214..5699442hg38UCSC Ensembl
Outerchr16:5529214..5699442hg38UCSC Ensembl
Innerchr16:5579215..5749443hg19UCSC Ensembl
Outerchr16:5579215..5749443hg19UCSC Ensembl
Innerchr16:5519216..5689444hg18UCSC Ensembl
Outerchr16:5519216..5689444hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38170229
hg19170229
hg18170229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784428
Samples
Known GenesMIR8065
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892765
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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