A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689818



Internal ID15055194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90917318..90918716hg38UCSC Ensembl
Innerchr15:90917716..90918318hg38UCSC Ensembl
Outerchr15:90916318..90919716hg38UCSC Ensembl
chr15:91460548..91461946hg19UCSC Ensembl
Innerchr15:91460946..91461548hg19UCSC Ensembl
Outerchr15:91459548..91462946hg19UCSC Ensembl
chr15:89261552..89262950hg18UCSC Ensembl
Innerchr15:89262552..89261950hg18UCSC Ensembl
Outerchr15:89260552..89263950hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3370257
Supporting Variants
SamplesNA19239
Known GenesMAN2A2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689818
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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