A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891380



Internal ID18839090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:31278415..31706814hg38UCSC Ensembl
Outerchr8:31278415..31706814hg38UCSC Ensembl
Innerchr8:31135931..31564330hg19UCSC Ensembl
Outerchr8:31135931..31564330hg19UCSC Ensembl
Innerchr8:31255473..31683872hg18UCSC Ensembl
Outerchr8:31255473..31683872hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38428400
hg19428400
hg18428400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792806
Samples
Known GenesNRG1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891380
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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