A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661802



Internal ID9927907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101085451..101090556hg38UCSC Ensembl
Outerchr15:101085414..101090606hg38UCSC Ensembl
Innerchr15:101625656..101630761hg19UCSC Ensembl
Outerchr15:101625619..101630811hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385193
hg195193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5958587
SamplesNA18621
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661802
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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