A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779357



Internal ID19178381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86268426..86331365hg38UCSC Ensembl
Innerchr16:86302032..86364971hg19UCSC Ensembl
Innerchr16:84859533..84922472hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3862940
hg1962940
hg1862940
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892931
Supporting Variants
Samples
Known GenesLINC01081, LOC146513
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779357
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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