A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672001



Internal ID9938106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107465320..107477471hg38UCSC Ensembl
chr11:107336046..107348197hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812152
hg1912152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5679034, essv5416127, essv6508653, essv5432021
SamplesNA19700, NA19371, NA19436, HG00312
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672001
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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