A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3441199



Internal ID15288152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35181406..35181425hg38UCSC Ensembl
Innerchr15:35181402..35181429hg38UCSC Ensembl
Outerchr15:35181383..35181448hg38UCSC Ensembl
chr15:35473607..35473626hg19UCSC Ensembl
Innerchr15:35473603..35473630hg19UCSC Ensembl
Outerchr15:35473584..35473649hg19UCSC Ensembl
chr15:33260899..33260918hg18UCSC Ensembl
Innerchr15:33260922..33260895hg18UCSC Ensembl
Outerchr15:33260876..33260941hg18UCSC Ensembl
Cytoband15q14
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 Variantsessv9668025, essv9668036, essv9668014
SamplesNA18970, NA11894, NA12043
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3441199
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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