A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891685



Internal ID19186081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78539585..78666999hg38UCSC Ensembl
Outerchr9:78539585..78666999hg38UCSC Ensembl
Innerchr9:81154501..81281915hg19UCSC Ensembl
Outerchr9:81154501..81281915hg19UCSC Ensembl
Innerchr9:80344321..80471735hg18UCSC Ensembl
Outerchr9:80344321..80471735hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38127415
hg19127415
hg18127415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792237
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891685
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