A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7735887



Internal ID14553073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70028999..70029093hg38UCSC Ensembl
Outerchr17:70028799..70029293hg38UCSC Ensembl
Innerchr17:68025140..68025234hg19UCSC Ensembl
Outerchr17:68024940..68025434hg19UCSC Ensembl
Innerchr17:65536735..65536829hg18UCSC Ensembl
Outerchr17:65536535..65537029hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38495
hg19495
hg18495
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303048
Supporting Variants
SamplesNA18949
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7735887
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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