A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7737859



Internal ID13807518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35772737..35772738hg38UCSC Ensembl
Outerchr4:35772590..35772886hg38UCSC Ensembl
Innerchr4:35774359..35774360hg19UCSC Ensembl
Outerchr4:35774212..35774508hg19UCSC Ensembl
Innerchr4:35450755..35450754hg18UCSC Ensembl
Outerchr4:35450607..35450903hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38297
hg19297
hg18297
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303016
Supporting Variants
SamplesNA18504
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7737859
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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