A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660562



Internal ID9926667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39466844..39479230hg38UCSC Ensembl
Outerchr15:39466807..39479280hg38UCSC Ensembl
Innerchr15:39759045..39771431hg19UCSC Ensembl
Outerchr15:39759008..39771481hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3812474
hg1912474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6228180
SamplesHG00473
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660562
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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