A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6048788



Internal ID9026191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121480607..121481951hg38UCSC Ensembl
chr11:121351316..121352660hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677977
Supporting Variants
SamplesNA19384
Known GenesSORL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6048788
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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