A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796335



Internal ID19176051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133071778..133082065hg38UCSC Ensembl
Innerchr9:135947165..135957452hg19UCSC Ensembl
Innerchr9:134936986..134947273hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3810288
hg1910288
hg1810288
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891731
Supporting Variants
Samples
Known GenesCEL
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796335
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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