A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9668014



Internal ID13184992
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 Flag1
Merged StatusS
Merged Variantsesv3441199
Supporting Variants
SamplesNA11894
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9668014
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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