A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662931



Internal ID9929036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76382002..76384738hg38UCSC Ensembl
Outerchr15:76381965..76384788hg38UCSC Ensembl
Innerchr15:76674343..76677079hg19UCSC Ensembl
Outerchr15:76674306..76677129hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5482852
SamplesHG00534
Known GenesSCAPER
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662931
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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