A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14297098



Internal ID4298914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122826302..122845342hg38UCSC Ensembl
chr11:122697010..122716050hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3819041
hg1919041
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627947
Supporting Variants
SamplesHG02325
Known GenesCRTAM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14297098
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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