A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7739107



Internal ID14830525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15945463..15947244hg38UCSC Ensembl
Outerchr4:15945263..15947444hg38UCSC Ensembl
Innerchr4:15947086..15948867hg19UCSC Ensembl
Outerchr4:15946886..15949067hg19UCSC Ensembl
Innerchr4:15556184..15557965hg18UCSC Ensembl
Outerchr4:15555984..15558165hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg382182
hg192182
hg182182
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303021
Supporting Variants
SamplesNA19099
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7739107
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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