A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808706



Internal ID13644380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74216410..74216850hg38UCSC Ensembl
Innerchr15:74216409..74216851hg38UCSC Ensembl
Outerchr15:74216300..74216970hg38UCSC Ensembl
chr15:74508751..74509191hg19UCSC Ensembl
Innerchr15:74508750..74509192hg19UCSC Ensembl
Outerchr15:74508641..74509311hg19UCSC Ensembl
chr15:72295804..72296244hg18UCSC Ensembl
Innerchr15:72296245..72295803hg18UCSC Ensembl
Outerchr15:72295694..72296364hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38441
hg19441
hg18441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3451538
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808706
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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