A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3419988



Internal ID15266946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31169096..31169115hg38UCSC Ensembl
Innerchr3:31169092..31169119hg38UCSC Ensembl
Outerchr3:31169073..31169138hg38UCSC Ensembl
chr3:31210588..31210607hg19UCSC Ensembl
Innerchr3:31210584..31210611hg19UCSC Ensembl
Outerchr3:31210565..31210630hg19UCSC Ensembl
chr3:31185592..31185611hg18UCSC Ensembl
Innerchr3:31185615..31185588hg18UCSC Ensembl
Outerchr3:31185569..31185634hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9608691, essv9608702
SamplesNA11918, NA18970
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3419988
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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