A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3373702



Internal ID15220677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36780808..36780808hg38UCSC Ensembl
Innerchr3:36780807..36780809hg38UCSC Ensembl
Outerchr3:36780758..36780858hg38UCSC Ensembl
chr3:36822299..36822299hg19UCSC Ensembl
Innerchr3:36822298..36822300hg19UCSC Ensembl
Outerchr3:36822249..36822349hg19UCSC Ensembl
chr3:36797303..36797303hg18UCSC Ensembl
Innerchr3:36797304..36797302hg18UCSC Ensembl
Outerchr3:36797253..36797353hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38578
hg19578
hg18578
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8741095
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3373702
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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