A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892649



Internal ID18836783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30905361..30918448hg38UCSC Ensembl
Outerchr15:30905361..30918448hg38UCSC Ensembl
Innerchr15:31197564..31210651hg19UCSC Ensembl
Outerchr15:31197564..31210651hg19UCSC Ensembl
Innerchr15:28984856..28997943hg18UCSC Ensembl
Outerchr15:28984856..28997943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3813088
hg1913088
hg1813088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786298
Samples
Known GenesFAN1, MIR7976
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892649
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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