A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7735698



Internal ID13542343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73999118..73999119hg38UCSC Ensembl
Outerchr11:73998950..73999288hg38UCSC Ensembl
Innerchr11:73710163..73710164hg19UCSC Ensembl
Outerchr11:73709995..73710333hg19UCSC Ensembl
Innerchr11:73387812..73387811hg18UCSC Ensembl
Outerchr11:73387643..73387981hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38339
hg19339
hg18339
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302949
Supporting Variants
SamplesNA12751
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7735698
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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