A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784428



Internal ID18828027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5529214..5699442hg38UCSC Ensembl
Innerchr16:5579215..5749443hg19UCSC Ensembl
Innerchr16:5519216..5689444hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38170229
hg19170229
hg18170229
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892765
Supporting Variants
Samples
Known GenesMIR8065
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=67
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784428
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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