A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891501



Internal ID19185897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:214864..355793hg38UCSC Ensembl
Outerchr9:112542..464920hg38UCSC Ensembl
Innerchr9:214864..355793hg19UCSC Ensembl
Outerchr9:112542..464920hg19UCSC Ensembl
Innerchr9:204864..345793hg18UCSC Ensembl
Outerchr9:102542..454920hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38352379
hg19352379
hg18352379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787808, essv25789720, essv25789275, essv25788133, essv25788370, essv25788091, essv25787934, essv25792837, essv25788271
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891501
Frequency
Sample Size3017
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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