A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307908



Internal ID15154856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38925486..38925487hg38UCSC Ensembl
Innerchr13:38925455..38925518hg38UCSC Ensembl
Outerchr13:38925454..38925519hg38UCSC Ensembl
chr13:39499623..39499624hg19UCSC Ensembl
Innerchr13:39499592..39499655hg19UCSC Ensembl
Outerchr13:39499591..39499656hg19UCSC Ensembl
chr13:38397623..38397624hg18UCSC Ensembl
Innerchr13:38397655..38397592hg18UCSC Ensembl
Outerchr13:38397591..38397656hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38162
hg19162
hg18162
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7838414, essv7838948, essv7837760, essv7837407
SamplesNA12891, NA19238, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307908
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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