A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14308026



Internal ID4309842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128701861..128712027hg38UCSC Ensembl
chr11:128571756..128581922hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3810167
hg1910167
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628048
Supporting Variants
SamplesHG03189
Known GenesFLI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14308026
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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