A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657314



Internal ID9576733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66414201..66414367hg38UCSC Ensembl
Innerchr15:66706539..66706705hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455e199
Supporting Variantsessv6269425, essv6577504, essv5589884
SamplesNA11931, NA12891, NA11831
Known GenesMAP2K1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657314
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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