A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3357710



Internal ID15204689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156660554..156660684hg38UCSC Ensembl
Innerchr4:156660561..156660677hg38UCSC Ensembl
Outerchr4:156660547..156660691hg38UCSC Ensembl
chr4:157581706..157581836hg19UCSC Ensembl
Innerchr4:157581713..157581829hg19UCSC Ensembl
Outerchr4:157581699..157581843hg19UCSC Ensembl
chr4:157801156..157801286hg18UCSC Ensembl
Innerchr4:157801163..157801279hg18UCSC Ensembl
Outerchr4:157801149..157801293hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38131
hg19131
hg18131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671195, essv8671197, essv8671194, essv8671192, essv8671191, essv8671193
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3357710
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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