A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689723



Internal ID15020903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28311211..28312709hg38UCSC Ensembl
Innerchr15:28311709..28312211hg38UCSC Ensembl
Outerchr15:28310211..28313709hg38UCSC Ensembl
chr15:28556357..28557855hg19UCSC Ensembl
Innerchr15:28556855..28557357hg19UCSC Ensembl
Outerchr15:28555357..28558855hg19UCSC Ensembl
chr15:26229952..26231450hg18UCSC Ensembl
Innerchr15:26230952..26230450hg18UCSC Ensembl
Outerchr15:26228952..26232450hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3409154
Supporting Variants
SamplesNA19238
Known GenesHERC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689723
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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