A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892674



Internal ID18836808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37311235..38400599hg38UCSC Ensembl
Outerchr15:37311235..38400599hg38UCSC Ensembl
Innerchr15:37603436..38692800hg19UCSC Ensembl
Outerchr15:37603436..38692800hg19UCSC Ensembl
Innerchr15:35390728..36480092hg18UCSC Ensembl
Outerchr15:35390728..36480092hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381089365
hg191089365
hg181089365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792148
Samples
Known GenesSPRED1, TMCO5A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892674
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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