A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667131



Internal ID9933236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65956094..65960448hg38UCSC Ensembl
Outerchr11:65955937..65960615hg38UCSC Ensembl
Innerchr11:65723565..65727919hg19UCSC Ensembl
Outerchr11:65723408..65728086hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384679
hg194679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6161290
SamplesHG00537
Known GenesTSGA10IP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667131
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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