A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778267



Internal ID19173449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59472207..59658722hg38UCSC Ensembl
Innerchr16:59506111..59692626hg19UCSC Ensembl
Innerchr16:58063612..58250127hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38186516
hg19186516
hg18186516
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892867
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778267
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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