A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892693



Internal ID18836827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50122688..50225890hg38UCSC Ensembl
Outerchr15:50120328..50225890hg38UCSC Ensembl
Innerchr15:50414885..50518087hg19UCSC Ensembl
Outerchr15:50412525..50518087hg19UCSC Ensembl
Innerchr15:48202177..48305379hg18UCSC Ensembl
Outerchr15:48199817..48305379hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38105563
hg19105563
hg18105563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789291, essv25789185
Samples
Known GenesSLC27A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892693
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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