A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636337



Internal ID7023131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45271734..45320801hg38UCSC Ensembl
Innerchr15:45271884..45320651hg38UCSC Ensembl
Outerchr15:45271584..45320951hg38UCSC Ensembl
chr15:45563932..45612999hg19UCSC Ensembl
Innerchr15:45564082..45612849hg19UCSC Ensembl
Outerchr15:45563782..45613149hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3849068
hg1949068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233831
SamplesNA19625
Known GenesSLC28A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636337
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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