A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14184929



Internal ID6848085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64408839..64445684hg38UCSC Ensembl
chr11:64176311..64213156hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3836846
hg1936846
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626660
Supporting Variants
SamplesNA21086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14184929
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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