A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797202



Internal ID19175744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91963384..91985134hg38UCSC Ensembl
Innerchr15:92506614..92528364hg19UCSC Ensembl
Innerchr15:90307618..90329368hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821751
hg1921751
hg1821751
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892723
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797202
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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