A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797623



Internal ID19161066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22739631..22790288hg38UCSC Ensembl
Innerchr9:22739630..22790287hg19UCSC Ensembl
Innerchr9:22729630..22780287hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3850658
hg1950658
hg1850658
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891635
Supporting Variants
Samples
Known GenesFLJ35282
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797623
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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