A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689754



Internal ID15054881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28657365..28658763hg38UCSC Ensembl
Innerchr15:28657763..28658365hg38UCSC Ensembl
Outerchr15:28656365..28659763hg38UCSC Ensembl
chr15:28902511..28903909hg19UCSC Ensembl
Innerchr15:28902909..28903511hg19UCSC Ensembl
Outerchr15:28901511..28904909hg19UCSC Ensembl
chr15:26701552..26702950hg18UCSC Ensembl
Innerchr15:26702552..26701950hg18UCSC Ensembl
Outerchr15:26700552..26703950hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3347385
Supporting Variants
SamplesNA19239
Known GenesHERC2P9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689754
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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