A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891628



Internal ID18839338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17269439..17280618hg38UCSC Ensembl
Outerchr9:17269439..17280618hg38UCSC Ensembl
Innerchr9:17269437..17280616hg19UCSC Ensembl
Outerchr9:17269437..17280616hg19UCSC Ensembl
Innerchr9:17259437..17270616hg18UCSC Ensembl
Outerchr9:17259437..17270616hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3811180
hg1911180
hg1811180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797341
Samples
Known GenesCNTLN
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891628
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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