A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637500



Internal ID7024292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101187713..101191362hg38UCSC Ensembl
Innerchr15:101187747..101191328hg38UCSC Ensembl
Outerchr15:101187679..101191396hg38UCSC Ensembl
chr15:101727918..101731567hg19UCSC Ensembl
Innerchr15:101727952..101731533hg19UCSC Ensembl
Outerchr15:101727884..101731601hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383650
hg193650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354133
SamplesNA20520
Known GenesCHSY1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637500
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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