A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891707



Internal ID18839417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105609268..105772991hg38UCSC Ensembl
Outerchr9:105609268..105772991hg38UCSC Ensembl
Innerchr9:108371549..108535272hg19UCSC Ensembl
Outerchr9:108371549..108535272hg19UCSC Ensembl
Innerchr9:107411370..107575093hg18UCSC Ensembl
Outerchr9:107411370..107575093hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38163724
hg19163724
hg18163724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790845
Samples
Known GenesFKTN, TAL2, TMEM38B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891707
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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