A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14246257



Internal ID2935464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97377934..97509631hg38UCSC Ensembl
chr11:97248934..97380631hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38131698
hg19131698
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627406
Supporting Variants
SamplesHG02594
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14246257
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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