A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292828



Internal ID5294644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74721538..74745196hg38UCSC Ensembl
Innerchr15:74721538..74745196hg38UCSC Ensembl
Outerchr15:74721447..74745274hg38UCSC Ensembl
chr15:75013879..75037537hg19UCSC Ensembl
Innerchr15:75013879..75037537hg19UCSC Ensembl
Outerchr15:75013788..75037615hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3823659
hg1923659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636907
Supporting Variants
SamplesHG03352
Known GenesCYP1A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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