A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636342



Internal ID7023136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45613973..45617386hg38UCSC Ensembl
Innerchr15:45613973..45617386hg38UCSC Ensembl
Outerchr15:45613766..45617604hg38UCSC Ensembl
chr15:45906171..45909584hg19UCSC Ensembl
Innerchr15:45906171..45909584hg19UCSC Ensembl
Outerchr15:45905964..45909802hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383414
hg193414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15235033
SamplesHG03079
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636342
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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