A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660680



Internal ID9580099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79898217..79960244hg38UCSC Ensembl
Outerchr15:79898180..79960294hg38UCSC Ensembl
Innerchr15:80190559..80252586hg19UCSC Ensembl
Outerchr15:80190522..80252636hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3862115
hg1962115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6292391
SamplesNA18627
Known GenesC15orf37, ST20, ST20-MTHFS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660680
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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