A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808714



Internal ID13644843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100710294..100710579hg38UCSC Ensembl
Innerchr15:100710293..100710580hg38UCSC Ensembl
Outerchr15:100710184..100710699hg38UCSC Ensembl
chr15:101250499..101250784hg19UCSC Ensembl
Innerchr15:101250498..101250785hg19UCSC Ensembl
Outerchr15:101250389..101250904hg19UCSC Ensembl
chr15:99068022..99068307hg18UCSC Ensembl
Innerchr15:99068308..99068021hg18UCSC Ensembl
Outerchr15:99067912..99068427hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38286
hg19286
hg18286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3446427
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808714
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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