A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3362106



Internal ID15209084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10308859..10308877hg38UCSC Ensembl
Innerchr18:10308854..10308880hg38UCSC Ensembl
Outerchr18:10308836..10308898hg38UCSC Ensembl
chr18:10308856..10308874hg19UCSC Ensembl
Innerchr18:10308851..10308877hg19UCSC Ensembl
Outerchr18:10308833..10308895hg19UCSC Ensembl
chr18:10298856..10298874hg18UCSC Ensembl
Innerchr18:10298877..10298851hg18UCSC Ensembl
Outerchr18:10298833..10298895hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38182
hg19182
hg18182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8972952, essv8972953, essv8972951, essv8972949, essv8972946, essv8972948, essv8972950
SamplesNA18870, NA18519, NA19138, NA18907, NA18523, NA19116, NA19129
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3362106
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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