A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14198525



Internal ID5183565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67742280..67808524hg38UCSC Ensembl
chr11:67509751..67575995hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3866245
hg1966245
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626721
Supporting Variants
SamplesNA18608
Known GenesFAM86C2P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14198525
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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