A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892928



Internal ID18837062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84354197..84448953hg38UCSC Ensembl
Outerchr16:84339110..84524557hg38UCSC Ensembl
Innerchr16:84387803..84482559hg19UCSC Ensembl
Outerchr16:84372716..84558163hg19UCSC Ensembl
Innerchr16:82945304..83040060hg18UCSC Ensembl
Outerchr16:82930217..83115664hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38185448
hg19185448
hg18185448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798342, essv25779434, essv25784684, essv25797439
Samples
Known GenesATP2C2, TLDC1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892928
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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