A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672678



Internal ID9938783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27539383..27551756hg38UCSC Ensembl
Outerchr11:27539346..27551806hg38UCSC Ensembl
Innerchr11:27560930..27573303hg19UCSC Ensembl
Outerchr11:27560893..27573353hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3812461
hg1912461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5554576
SamplesHG00614
Known GenesBDNF-AS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672678
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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