A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307004



Internal ID15153952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32297906..32297907hg38UCSC Ensembl
Innerchr3:32297884..32297929hg38UCSC Ensembl
Outerchr3:32297883..32297930hg38UCSC Ensembl
chr3:32339398..32339399hg19UCSC Ensembl
Innerchr3:32339376..32339421hg19UCSC Ensembl
Outerchr3:32339375..32339422hg19UCSC Ensembl
chr3:32314402..32314403hg18UCSC Ensembl
Innerchr3:32314425..32314380hg18UCSC Ensembl
Outerchr3:32314379..32314426hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38661
hg19661
hg18661
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7767706
SamplesNA11918
Known GenesCMTM8
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307004
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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