A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660587



Internal ID9926692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38743016..38761722hg38UCSC Ensembl
Outerchr11:38742645..38762092hg38UCSC Ensembl
Innerchr11:38764566..38783272hg19UCSC Ensembl
Outerchr11:38764195..38783642hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3819448
hg1919448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5792864, essv5636478, essv6563109
SamplesNA19130, NA18874, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660587
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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