A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3353496



Internal ID14853760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134073018..134075316hg38UCSC Ensembl
Innerchr3:134074018..134074316hg38UCSC Ensembl
Outerchr3:134072018..134076316hg38UCSC Ensembl
chr3:133791862..133794160hg19UCSC Ensembl
Innerchr3:133792862..133793160hg19UCSC Ensembl
Outerchr3:133790862..133795160hg19UCSC Ensembl
chr3:135274552..135276850hg18UCSC Ensembl
Innerchr3:135275552..135275850hg18UCSC Ensembl
Outerchr3:135273552..135277850hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8693850
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3353496
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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