A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7768371



Internal ID13616673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36083015..36083016hg38UCSC Ensembl
Innerchr13:36082993..36083038hg38UCSC Ensembl
Outerchr13:36082992..36083039hg38UCSC Ensembl
chr13:36657152..36657153hg19UCSC Ensembl
Innerchr13:36657130..36657175hg19UCSC Ensembl
Outerchr13:36657129..36657176hg19UCSC Ensembl
chr13:35555152..35555153hg18UCSC Ensembl
Innerchr13:35555175..35555130hg18UCSC Ensembl
Outerchr13:35555129..35555176hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38296
hg19296
hg18296
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303266
Supporting Variants
SamplesNA12872
Known GenesDCLK1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7768371
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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