A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6315316



Internal ID9670065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42251335..42254211hg38UCSC Ensembl
chr11:42272885..42275761hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670858
Supporting Variants
SamplesNA19399
Known GenesLOC100507205
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6315316
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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