A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891716



Internal ID18839426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113098921..113152914hg38UCSC Ensembl
Outerchr9:113098921..113152914hg38UCSC Ensembl
Innerchr9:115861201..115915194hg19UCSC Ensembl
Outerchr9:115861201..115915194hg19UCSC Ensembl
Innerchr9:114901022..114955015hg18UCSC Ensembl
Outerchr9:114901022..114955015hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3853994
hg1953994
hg1853994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797800
Samples
Known GenesFAM225A, FAM225B, SLC31A2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891716
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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