A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7736526



Internal ID14964807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147967616..147967628hg38UCSC Ensembl
Outerchr3:147967416..147967828hg38UCSC Ensembl
Innerchr3:147685403..147685415hg19UCSC Ensembl
Outerchr3:147685203..147685615hg19UCSC Ensembl
Innerchr3:149168093..149168105hg18UCSC Ensembl
Outerchr3:149167893..149168305hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38413
hg19413
hg18413
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302769
Supporting Variants
SamplesNA19190
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7736526
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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