A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5554576



Internal ID9006993
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 Flag1
Merged StatusS
Merged Variantsesv2672678
Supporting Variants
SamplesHG00614
Known GenesBDNF-AS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5554576
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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