A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891728



Internal ID18839438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129234668..129241234hg38UCSC Ensembl
Outerchr9:129233792..129242284hg38UCSC Ensembl
Innerchr9:131996947..132003513hg19UCSC Ensembl
Outerchr9:131996071..132004563hg19UCSC Ensembl
Innerchr9:131036768..131043334hg18UCSC Ensembl
Outerchr9:131035892..131044384hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388493
hg198493
hg188493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801166, essv25785463, essv25796166, essv25796453, essv25796461, essv25779104
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891728
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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