A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636907



Internal ID6677014
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292826, essv15292827, essv15292828
SamplesHG03199, HG03352, HG03108
Known GenesCYP1A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636907
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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