A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796009



Internal ID19162267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107800122..107857699hg38UCSC Ensembl
Innerchr13:108452470..108510047hg19UCSC Ensembl
Innerchr13:107250471..107308048hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3857578
hg1957578
hg1857578
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892444
Supporting Variants
Samples
Known GenesFAM155A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796009
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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