A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797341



Internal ID18835830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17269439..17280618hg38UCSC Ensembl
Innerchr9:17269437..17280616hg19UCSC Ensembl
Innerchr9:17259437..17270616hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3811180
hg1911180
hg1811180
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891628
Supporting Variants
Samples
Known GenesCNTLN
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797341
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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