A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304772



Internal ID15151720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157651332..157651333hg38UCSC Ensembl
Innerchr3:157651315..157651350hg38UCSC Ensembl
Outerchr3:157651314..157651351hg38UCSC Ensembl
chr3:157369121..157369122hg19UCSC Ensembl
Innerchr3:157369104..157369139hg19UCSC Ensembl
Outerchr3:157369103..157369140hg19UCSC Ensembl
chr3:158851815..158851816hg18UCSC Ensembl
Innerchr3:158851833..158851798hg18UCSC Ensembl
Outerchr3:158851797..158851834hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38207
hg19207
hg18207
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7775249, essv7784272, essv7806278, essv7796864, essv7832990, essv7778709, essv7792223, essv7774056, essv7781342, essv7789449, essv7806094, essv7825806, essv7836360, essv7782054, essv7815834, essv7809740, essv7795233, essv7802188, essv7832203, essv7791660, essv7811639, essv7811203, essv7818345, essv7825246
SamplesNA19141, NA18508, NA18507, NA12004, NA18504, NA19190, NA18870, NA18510, NA19138, NA11994, NA19210, NA12872, NA18871, NA18856, NA18912, NA19099, NA19257, NA19108, NA19147, NA18517, NA19093, NA18505, NA19129, NA18522
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304772
Frequency
Sample Size185
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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