A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3377638



Internal ID15224611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40808112..40808131hg38UCSC Ensembl
Innerchr15:40808108..40808135hg38UCSC Ensembl
Outerchr15:40808089..40808154hg38UCSC Ensembl
chr15:41100310..41100329hg19UCSC Ensembl
Innerchr15:41100306..41100333hg19UCSC Ensembl
Outerchr15:41100287..41100352hg19UCSC Ensembl
chr15:38887602..38887621hg18UCSC Ensembl
Innerchr15:38887625..38887598hg18UCSC Ensembl
Outerchr15:38887579..38887644hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9668291, essv9668369, essv9668302, essv9668324, essv9668313, essv9668336, essv9668347, essv9668358
SamplesNA19141, NA12045, NA12812, NA11918, NA12815, NA12872, NA12234, NA11840
Known GenesZFYVE19
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3377638
Frequency
Sample Size185
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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