A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5946308



Internal ID8923711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13962055..14027138hg38UCSC Ensembl
chr11:13983602..14048685hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3865084
hg1965084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668036
Supporting Variants
SamplesHG00702
Known GenesSPON1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5946308
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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