A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663545



Internal ID9582964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89516184..89518431hg38UCSC Ensembl
Outerchr15:89516027..89518584hg38UCSC Ensembl
Innerchr15:90059415..90061662hg19UCSC Ensembl
Outerchr15:90059258..90061815hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382558
hg192558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5444345, essv6038760
SamplesHG00337, HG00178
Known GenesLINC00928
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663545
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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