A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15319555



Internal ID5054789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92025748..92028504hg38UCSC Ensembl
Innerchr15:92025748..92028504hg38UCSC Ensembl
Outerchr15:92025630..92028646hg38UCSC Ensembl
chr15:92568978..92571734hg19UCSC Ensembl
Innerchr15:92568978..92571734hg19UCSC Ensembl
Outerchr15:92568860..92571876hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382757
hg192757
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637252
Supporting Variants
SamplesNA18533
Known GenesSLCO3A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15319555
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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