A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892931



Internal ID19183751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86268525..86331365hg38UCSC Ensembl
Outerchr16:86268426..86331365hg38UCSC Ensembl
Innerchr16:86302131..86364971hg19UCSC Ensembl
Outerchr16:86302032..86364971hg19UCSC Ensembl
Innerchr16:84859632..84922472hg18UCSC Ensembl
Outerchr16:84859533..84922472hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3862940
hg1962940
hg1862940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798495, essv25779357
Samples
Known GenesLINC01081, LOC146513
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892931
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer